The Selection and Use of Essential Medicines

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This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the World Health Organization WHO Technical Report Series 933

THE SELECTION AND USE OF ESSENTIAL MEDICINES

Report of the WHO Expert Committee, 2005 (including the 14th Model List of Essential Medicines)

World Health Organization Geneva 2006

i WHO Library Cataloguing-in-Publication Data

WHO Expert Committee on the Selection and Use of Essential Medicines (14th : 2005: Geneva, Switzerland) The selection and use of essential medicines : report of the WHO Expert Committee, 2005 : (including the 14th model list of essential medicines).

(WHO technical report series ; 933)

1.Essential drugs — standards 2.Formularies — standards 3.Drug information services — organization and administration 4.Drug utilization 5. Pharmaceutical preparations — classification 6.Guidelines I.Title II.Title: 14th model list of essential medicines III.Series.

ISBN 92 4 120933 X (LC/NLM classification: QV 55) ISSN 0512-3054

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This publication contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the World Health Organization.

Typeset in China, Hong Kong Special Administrative Region Contents

1. Introduction 1

2. Open session 2

3. Update on current activities on selection and rational use 3 3.1 Dissemination of the previous report of the Expert Committee (including the 13th Model List) 3 3.2 WHO Model Formulary and WHO Essential Medicines Library 4 3.3 Plans for further revisions of the Model List and WHO model formulary 4 3.4 Review of essential medicines for reproductive health 5 3.5 Review of the Interagency Emergency Health Kit 2005 5 3.6 Report of the WHO Advisory Committee on Safety of Medicinal Products 6 3.7 Update on current activities in the field of rational use of medicines 6 3.8 Report of the Critically Important Antibiotics for Human Health Meeting, Canberra, Australia, 15–17 February 2005 7 3.9 Update on the Priority Medicines Project 8 3.10 Collaboration with the International Society of Drug Bulletins 8 3.11 Discussion 8

4. Changes made in revising the Model List 9 4.1 Applications for deletions 9 4.1.1 Aminophylline and theophylline 9 4.1.2 Atropine 10 4.1.3 Calcium gluconate 10 4.1.4 Clonazepam 11 4.1.5 Codeine 11 4.1.6 Colchicine 12 4.1.7 Cromoglycic acid 12 4.1.8 Diethyltoluamide 13 4.1.9 Ergotamine 13 4.1.10 Ergometrine 14 4.1.11 Ether 14 4.1.12 Factors VIII and IX concentrates 15 4.1.13 Imipenem + cilastatin 16 4.1.14 Isoprenaline 17 4.1.15 Levofloxacin 17 4.1.16 Local anaesthetic, astringent or anti-inflammatory as antihaemhorrhoidal medicines 18 4.1.17 Medroxyprogesterone acetate (depot injection 150mg/ml) 18 4.1.18 Medroxyprogesterone acetate (tablet 5mg) 19 4.1.19 Nalidixic acid 19 4.1.20 Niclosamide 20 4.1.21 Nifedipine 20 4.1.22 Oxamniquine 21

iii 4.1.23 Polygeline 21 4.1.24 Procainamide 22 4.1.25 Pyrantel 22 4.1.26 Quinidine 23 4.1.27 Salbutamol 23 4.1.28 Silver nitrate eye solution 23 4.1.29 Sodium fluoride 24 4.1.30 Spectinomycin 24 4.1.31 Sun protection agents 25 4.1.32 Thioacetazone + isoniazid 25 4.1.33 Triclabendazole 27 4.2 Applications for additions 27 4.2.1 Caffeine citrate 27 4.2.2 Cefixime 28 4.2.3 Clotrimazole 28 4.2.4 Combination injectable contraceptives 29 4.2.5 Emtricitabine 29 4.2.6 Emtricitabine + tenofovir fixed-dose combination 30 4.2.7 Etonogestrel-releasing implant 30 4.2.8 Ibuprofen paediatric suspension 31 4.2.9 Levonorgestrel-releasing implant 32 4.2.10 Levonorgestrel-releasing IUD 32 4.2.11 Methadone and buprenorphine 33 4.2.12 Methoxyflurane 34 4.2.13 Miltefosine 35 4.2.14 Nifedipine 35 4.2.15 Mifepristone with misoprostol 36 4.2.16 Misoprostol, low dose 37 4.2.17 Nifedipine 38 4.2.18 Tenofovir 38 4.2.19 Zinc sulfate 39 4.3 Other changes 40 4.3.1 Alcuronium and vecuronium 40 4.3.2 Antiretroviral medicines 40 4.3.3 Ceftriaxone 1g injection 41 4.3.4 Immunoglobulin, human normal 41 4.3.5 Labetalol 42 4.3.6 Prostaglandins for postpartum haemorrhage 43

5. Reviews of sections of the Model List 43 5.1 Beta-lactam medicines 43 5.2 General anaesthetics and oxygen 44 5.3 Muscle relaxants 44 5.4 Ophthalmological preparations 44

6. Rare diseases 44

7. Future priorities 45 7.1 Summary of recommendations — additions, changes and deletions to the Model List 45 7.2 Methodological issues 48 7.3 Rational medicine use 48 iv References 49

Annex 1 The 14th WHO Model List of Essential Medicines 54

Annex 2 The Anatomical Therapeutic Chemical (ATC) classification system 93

Alphabetical list of essential medicines (with ATC classiﬁcation code numbers) 112

v WHO Expert Committee on the Selection and Use of Essential Medicines Geneva, 7–11 March 2005

Members Dr T.I. Bhutta, International Paediatric Association, Lahore, Pakistan Dr P.M. de Buschiazzo, Department of Pharmacology, School of Medicine, Univer- sity of La Plata, La Plata, Argentina Dr A. Helali, Director, Centre National de Pharmacovigilance et Matériovigilance, Ministère de la Santé et de la Population, Algiers, Algeria Dr S. Hill, Department of Clinical Pharmacology, University of Newcastle, New South Wales, Australia (Rapporteur) Dr J.-R. Laporte, Department of Pharmacology and Therapeutics, Fundacio Institut Català de Farmacologia, Universitat Autonoma de Barcelona, Barcelona, Spain (Chairman) Mr D. Mehta, Executive Editor, British National Formulary, Royal Pharmaceutical Society of Great Britain, London, England Dr E.M.A. Ombaka, Coordinator, Ecumenical Pharmaceutical Network, Nairobi, Kenya Dr Marcus M. Reidenberg, Chief, Division of Clinical Pharmacology, Weill Medical College of Cornell University, New York, NY, USA Dr S. Suryawati, Department of Clinical Pharmacology, Centre for Clinical Phar- macology and Drug Policy Studies, Gadjah Mada University, Yogyakarta, Indonesia Dr L. Wannmacher, Department of Clinical Pharmacology, School of Medicine, University of Passo Fundo, Passo Fundo, Rio Grande do Sul, Brazil Dr L. Ziganshina, Kazan State Medical Academy, Department of Clinical Pharma- cology and Pharmacotherapy, Kazan, Russian Federation

Representatives of other organizations* Joint United Nations Programme on HIV/AIDS Dr Julian Fleet, Senior Adviser, Care and Public Policy, UNAIDS, Geneva, Switzerland

United Nations Children’s Fund (UNICEF) Ms T. Huong Ha, Pharmaceuticals and Micronutrients, Supply Division UNICEF, Copenhagen, Denmark

United Nations Population Fund (UNFPA) Dr G. Walker, Director, Country Services Team for Eastern Europe and Central Asia, Bratislava, Slovakia Dr Vincent Fauveau, Maison Internationale de l’environnement, Chatelaine, Geneva, Switzerland

* Unable to attend: the World Bank and the WHO Collaborating Cetre for International Drug Monitoring. vi Secretariat Dr L.A. Bero, University of California at San Franscisco, San Francisco, CA, USA (Temporary Adviser) Dr J. Collier, International Society of Drug Bulletins, Medicines Policy Unit, Pharma- cology and Clinical Pharmacology, St George’s Hospital Medical School, London, England ( Temporary Adviser) Dr L.G. Cuervo-Amore, Clinical Evidence, BMA House, London, England (Tempo- rary Adviser) Dr A. Gray, Department of Experimental and Clinical Pharmacology, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Congella, South Africa (Temporary Adviser) Dr R. Gray, Medical Officer, Policy, Access and Rational Use, Department of Medicines Policy and Standards, WHO, Geneva, Switzerland Dr U. Gupta, Delhi Society for Promotion of Rational Use Of Drugs, National Institute of Immunology, New Delhi, India (Temporary Adviser) Dr H.V. Hogerzeil, Director, Department of Medicines Policy and Standards, WHO, Geneva, Switzerland (Secretary) Dr R.O. Laing, Medical Officer, Policy Access and Rational Use, Department of Medicines Policy and Standards, WHO, Geneva, Switzerland Dr V.K. Lepakhin, Assistant Director-General, Health Technology and Pharmaceu- ticals (HTP Cluster), WHO, Geneva, Switzerland Dr Y. Li, Chinese Cochrane Centre, West China Hospital, Sichuan University, Chengdu, People’s Republic of China (Temporary Adviser) Dr A.G. Miranda, HIV-TB Care and Treatment Team, Global AIDS Program, Na- tional Centers for HIV, STD and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA (Temporary Adviser) Dr G. Mignot, la revue Prescrire, Paris, France (Temporary Adviser) Ms W. Yoongthong, Senior Pharmacist, Food and Drug Administration, Bangkok, Thailand Dr Ogori Taylor, Yaba, Lagos, Nigeria

vii

1. Introduction The WHO Expert Committee on the Selection and Use of Essential Medicines met in Geneva from 7 to 11 March 2005. The meeting was opened on behalf of the Director-General by Dr V.K. Lepakhin, Assistant Director-General for Health Technology and Pharmaceuti- cals. He stated that WHO’s medicines programme is very important to Member States and that the recommendations made by its Expert Committees were critical. He explained that the Department of Essential Drugs and Medicines Policy had recently been divided into two new departments. The Department of Medicines Policy and Standards would focus on policy and normative work, whereas the Department of Technical Cooperation for Essential Drugs and Tradi- tional Medicines would concentrate on country support. Both departments would collaborate closely within one area of work, called Essential Medicines. Dr Lepakhin expressed appreciation to the staff of the Department of Essential Drugs and Medicines Policy for its hard work of the past year despite the uncertainties regarding the new structure.

Dr H.V. Hogerzeil, Director of the Department of Medicines Policy and Standards, and Secretary of the Expert Committee, also welcomed the participants. He noted that this would be the third Expert Committee operating under the new procedures approved in 2002. The full effect of these new procedures was now apparent in the careful and timely presentation of evidence-based applications for additions, changes or deletions to the WHO Model List of Essential Medicines (the Model List). Early web posting of most documents, together with the rounds of review and comments prior to the meeting ensured the transparency of the process.

The WHO Secretariat requested and received agreement from the Committee to hold an open session as part of its meeting (see section 2). The purpose of the open session was to allow all stakeholders to participate in the discussions and to comment on issues relating to the WHO Model List of Essential Medicines. Furthermore, for Expert Committee members it provides an opportunity to receive, at ﬁrst- hand, additional information and opinion on matters under consideration. Discussion and consideration of the open session are reﬂected in the report of the meeting.

The Committee decided to maintain the reporting format adopted at previous meetings. A summary of the Committee’s considerations on each of the items under discussion is presented in the main body of the report. The updated version of the Model List (the 14th Model

1 List), including a general introduction and explanatory notes, is presented in Annex 1. This Annex is also posted on the WHO web site and printed in hard copy in all six ofﬁcial languages of the Organiza- tion. A list of items on the Model List ordered by their corresponding Anatomical Therapeutical Chemical (ATC) classiﬁcation code number(s) is attached as Annex 2. The full texts of the applications for changes, additions or deletions with all the evidence and references, as well as the external reviews and comments received, are not included in the report but remain available on the WHO web site, and are accessible through the Essen- tial Medicines Library (http://mednet3.who.int/EMLib/). Information on medicines deleted from the Model List in the past is retained in a separate section of the library.

2. Open session The session was opened by Dr H.V. Hogerzeil, Director of the De- partment of Medicines Policy and Standards, and Secretary of the Expert Committee. He brieﬂy explained some aspects regarding the procedures of the Committee. He explained that the Committee is not a representative committee, that all members participate in their personal capacity and are not allowed to take instructions from any government or any other authority. He also stated that all information submitted to the Committee in support of the evidence-based decisions would be placed in the public domain through the WHO web site. This was especially important because in one case an applicant had not allowed unpublished materials which had been referred to in the original application to be posted on the web site, although these materials had been made available to the reviewers. In this case the applicant was requested to resubmit the application on the basis of information that could be placed in the public domain. Dr Hogerzeil reminded participants that all comments made during the open session would be noted and taken into consideration by the Committee when formulating ﬁnal recommendations in subsequent private sessions. As part of the open session, participants were briefed about various activities relating to the Model List and the rational use of medicines (see section 3.7). The new methodology used to have systematic reviews of sections of the Model List performed by experts from various national and other medicine bulletins was also summarized. A number of issues were raised and debated during the open session. Two representatives of the World Federation of Hemophilia,

2 including the President, made a presentation in support of their request that factor VIII and factor IX be retained on the Model List. The core arguments were that haemophilia can easily be diagnosed, that treatment is life-saving and easy to administer, that the use of alternative products would increase the risk of transmission of blood- borne viruses, and that deleting these medicines from the Model List would seriously jeopardize global efforts to make the treatment more widely available to all who need it. Médecins Sans Frontières called for all data supporting the application for recent antiretroviral (ARV) medicines to be made available to the Committee, and requested WHO to update its treatment protocols for human immunodeﬁciency virus/acquired immuno- deﬁciency syndrome (HIV/AIDS) in developing countries. A staff member from the Quality Assurance and Safety of Medicines team, WHO, cautioned against the inclusion of methadone and buprenorphine for the treatment of drug dependence, because of the risk of diversion.

3. Update on current activities on selection and rational use Dr H.V. Hogerzeil informed the Committee of the following recent activities.

3.1 Dissemination of the previous report of the Expert Committee (including the 13th Model List) Members approved the report of the previous meeting of the Expert Committee for publication by the Director-General and for posting on the WHO web site within two weeks of the meeting. In 2004 the full report was issued in the WHO Technical Report Series (1), in English. The 13th Model List and the general introduction (Annex 1 of the report) were posted on the WHO web site within weeks of the meeting, in all six ofﬁcial languages (Arabic, Chinese, English, French, Russian and Spanish). Hard copies of Annex 1 in English, French and Spanish were printed and widely distributed. An- nouncements of the new information on the WHO web site were made through international e-mail networks in English, French, Spanish and Russian to over 5000 experts and stakeholders worldwide.

3 3.2 WHO Model Formulary and WHO Essential Medicines Library The changes to the 13th Model List of 2003 were incorporated into a second edition of the WHO model formulary, which was issued in January 2004 as the WHO model formulary 2004 (2). This version is now available in hard copy and as a searchable database within the WHO Essential Medicines Library on the WHO web site. The database version is also available as a CD-ROM. A brief technical manual has been developed and added to the CD-ROM version to guide national formulary committees when developing a national formulary using the WHO model formulary (3). A Spanish-language version of the WHO model formulary is available in hard copy, on the web site and as a CD-ROM. Arabic and Russian translations have been completed and will soon be issued on the web site and as CD-ROMs. A special software program is being used for tracking any changes made in updating the original English text of the WHO model formulary, to facilitate updating the translations. The WHO Medicines Library on the WHO web site has been further developed. It now incorporates the Model List, the WHO model formulary, references and electronic links to most clinical guidelines developed by WHO, price information, nomenclature and links to information on quality and standards. The “Medicines Bookshelf”, a CD-ROM containing more than 250 key WHO publications on pharmaceuticals in all available language versions, also contains a digital version of the Essential Medicines Library.

3.3 Plans for further revisions of the Model List and WHO model formulary In view of the considerable time and resources needed to organize the Expert Committee, produce the report and the Model List, and adapt and translate the WHO model formulary into various languages, a two-year production cycle has been chosen, the early experience with which is very positive. This approach implies that the Expert Commit- tee will meet in Spring in alternate years (starting from Model List 2003). The report and the new Model List are then issued in the course of the same year. At the same time, the necessary changes are reﬂected in the next edition of the WHO model formulary, which is issued in January of the following year. Translations of the WHO model formulary follow as soon as possible, using the system to track the changes made, and focusing on electronic publication, which is both inexpensive and rapid. In early 2005 the revision of the Model List takes place, followed by the update of the WHO model formulary in 2006.

4 3.4 Review of essential medicines for reproductive health The overall objective of the Quality Medicines for Reproductive Health Project is to improve access to essential reproductive health (RH) medicines and commodities by promoting global standards, developing guidance on assured quality suppliers and products, and building procurement capacity in resource-limited countries. In the past year, interagency consultations had been held between United Nations (UN) agencies and nongovernmental organizations (NGOs) working in the field of RH to finalize jointly the Essential List for RH medicines and commodities. Discrepant medicines1 on UN RH lists were identified and decisions made (based on preliminary reviews) either to delete them from all RH lists and guidelines or to review them formally for possible addition to the Model List. For example, tinidazole will be deleted from the clinical guidelines as metronidazole is the first-line treatment for trichomoniasis. Other medicines, such as cefixime and misoprostol, were formally submitted and reviewed for possible addition to the WHO Model List of Essential Medicines. Sixteen RH medicines were reviewed during the 14th Expert Committee Meeting on the Selection and Use of Essential Medicines. Discrepancies in terminology and content of non-medicine items in existing RH lists have also been documented and a workplan towards finalization of the harmonized UN Reproductive Health Medicines and Devices List has been formulated. As soon as the lists of essential RH medicines and of essential RH devices are finalized, RH standard treatment guidelines will be updated accordingly. These model treatment guidelines and the list of essential RH items will be made available to national programmes with guidelines to help national RH programme officers increase inclusion of RH medicines on national lists of essential medicines.

3.5 Review of the Interagency Emergency Health Kit Review of the New Emergency Health Kit 1998 is in progress. Three interagency meetings have been held and decisions have been made to change the name of the kit and to maintain the structure of 10 basic units and a single supplementary unit. As the default position it has been decided that kits should contain treatment for malaria and for

1 A discrepant medicine is a medicine listed on one list but not on another. The three lists reviewed to check for discrepancies were: The 13th WHO Model List of Essential Medicines, 2003 (EML), the draft United Nations Population Fund (UNFPA)/WHO List of Essential Drugs and Commodities for Reproductive Health Services, 2003 (UNFPA list) and the Draft Interagency UNFPA/United Nations Population Fund (UNAIDS)/WHO Reproductive Health Medicines and Commodities List, 2002 (RHMCL).

5 the presumptive treatment of victims of sexual violence unless speciﬁc requests are made by purchasers not to provide them. Basic units will contain artemether + lumefantrine with rapid diagnostic tests for malaria. Other additions, changes and deletions have been agreed. The place of sulfamethoxazole + trimethoprim in the basic units is under discussion because of increasing reports of resistance to this combination. It is anticipated that there will be interagency agreement on the contents of the kit, which will be posted on the Medicines web site and will be followed by a document later in 2006.

3.6 Report of the WHO Advisory Committee on Safety of Medicinal Products The aims of pharmacovigilance are to promote patient care and patient safety, especially with regard to the prevention of unintended harm from the use of medicines. It also aims to improve public health and safety by the provision of reliable, balanced information, which will contribute to the assessment of the risk–benefit profile of medicines, and, in turn, encourage safer and more effective use of medicines. To promote these aims of pharmacovigilance, WHO has established a high-level Advisory Committee on Safety of Medicinal Products (ACSoMP). The second meeting of this Committee was held in Octo- ber 2004. Major items on the agenda were the recent establishment of the International Alliance for Patient Safety, the safety of medicines for children, pharmacovigilance in various public health programmes, and in relation to several specific medicines. The Advisory Commit- tee expressed a strong interest in contributing to the work of the Expert Committee.

3.7 Update on current activities in the ﬁeld of rational use of medicines WHO continues to develop and expand the medicine use database, which now contains more than 550 studies. The database provides useful data to track use of medicines over time, and between sectors and prescriber types in developing and transitional countries. The data will be used for planning, evaluation and advocacy. The manual Drug and therapeutics committees: a practical guide was published in April 2004, and French and Spanish versions are due for publication in 2006. Four international and seven national courses have been conducted in Africa, Asia and Latin America, during which 361 people from 56 countries have been trained in drug and therapeutics committee activities. Such committees can be promoted

6 in developing countries through a combination of training and follow- up support. In April 2004, as part of a global effort to improve the use of medicines, 472 leading policy-makers, researchers and other stakeholders representing 70 countries gathered again in Chiang Mai, Thailand, for the Second International Conference on Improving Use of Medicines (ICIUM 2004). This conference was supported by WHO and other partners. Evidence presented made it clear that despite examples of progress, misuse of medicines continues to be widespread and has serious health and economic implications, especially in resource-poor settings. Participants called upon governments to implement policies and programmes in the priority areas discussed at the conference. (All conference presentations, posters and abstracts are available at http://www.icium.org.) Many promising and successful interventions were presented at ICIUM 2004, yet global progress so far, has been conﬁned primarily to demonstration projects. There are few reports of effective national efforts to improve the use of medicines on a large scale and in a sustainable manner. The conference therefore highlighted the need to move from small-scale research projects to implementing programmes that achieve large-scale and sustained improvements within health systems. WHO has also been working towards containing antimicrobial resistance (AMR) through advocacy at the country, regional and global levels. Five operational research projects in India and South Africa are being supported to develop community-based surveillance systems. The initial results were presented at ICIUM 2004, where it was concluded that it is possible to have a locally-based multidisciplinary approach to contain AMR in a resource-poor setting. There is an urgent need for further research and other activities in this area. A resolution on AMR is being submitted to the 2005 World Health Assembly.

3.8 Report of the Critically Important Antibiotics for Human Health Meeting, Canberra, Australia, 15–17 February 2005 Antibiotic resistance arising from non-human use of antibacterial agents contributes to the resistance burden in humans. WHO is participating in efforts to establish a list of antibacterial agents, for which loss of efﬁcacy resulting from bacterial resistance would be disastrous to human medicine. This list will subsequently be used by the Codex Alimentarius Commission in deﬁning risk management strategies for non-human use of antibacterial agents. Two criteria were used to

7 categorize antibacterials: (1) the antibacterial is the sole therapy, or one of few alternatives, available to treat serious human disease, or (2) the antibacterial is used to treat diseases caused by bacteria that may be transmitted, or acquire resistance genes, from non-human sources. Antibacterials that met both criteria were categorized as critically important; antibacterials that met one criterion were categorized as highly important and antibacterials that met neither criterion were categorized as important. The great majority of the antibacterials on the Model List were considered to be critically important. The sulfonamides, doxycycline and spectinomycin were considered highly important. Cloxacillin, chloramphenicol, clindamycin, metronidazole and nitrofurantoin were considered important.

3.9 Update on the Priority Medicines Project In response to a request and support provided by the Government of the Netherlands, WHO has produced a report on Priority medicines for Europe and the world (4). This report reviewed the global and European burden of diseases; assessed where pharmaceutical gaps existed; suggested areas in which pharmaceutical innovation was required; and attempted to identify future essential medicines. In addition, the report addressed the particular needs of children, women, the elderly and those suffering from rare diseases. A section of the report addressed barriers to innovation in relation to regulatory and pricing issues, and the need for comparative clinical trials. A series of conclusions and recommendations was also provided. The report was presented at a major meeting of the European Union in The Hague on 18 November 2004 and will be used as a resource for the seventh framework programme of the European Community for research, technological development and demonstration activities.

3.10 Collaboration with the International Society of Drug Bulletins A report was given by the Chair of the International Society of Drug Bulletins (ISDB) on a WHO/ISDB pilot project to write three section reviews and to review 21 single medicines previously identiﬁed for possible deletion from the Model List at the Expert Committee meeting of 2003. The completed reviews were posted on the WHO web site as part of the documentation to be used by the Expert Committee in its deliberations.

3.11 Discussion The Committee considered that there was great potential for collaboration with the WHO Advisory Committee on Safety of Medicinal

8 Products. One issue noted was the potential difﬁculty in accessing data on adverse reactions from the WHO Collaborating Centre for International Drug Monitoring because of the Centre’s need to raise resources for its work on a “user-pays” basis. The Committee noted the importance of ensuring sufﬁcient resources to support the work of the Advisory Committee and the Collaborating Centre. The Commit- tee looked forward to further collaboration with the Advisory Com- mittee in relation to medicines on the Model List. The Committee noted the report by the Secretariat entitled “Rational use of medicines by prescribers and patients” provided for the provisional agenda of the 115th Session of the Executive Board and the Executive Board Resolution “Antimicrobial resistance: a threat to global health security”. The Committee considered that the Reso- lution, although it addresses a critically important public health issue, was focused on antimicrobial resistance and did not address the equally critical issues of developing strategies to improve the use of medicines in general. The Committee therefore strongly recommended that WHO encourage and support Member States in developing and implementing effective strategies (5) and national programmes to improve access to and quality use of medicines. Fur- thermore, the Committee recommended that WHO urgently identify potential sources of funding and donor support to develop a workplan for this key area.

4. Changes made in revising the Model List

4.1 Applications for deletions 4.1.1 Aminophylline and theophylline During its meeting in 2003, the Committee recommended that aminophylline and theophylline be reviewed for fast-track deletion at the meeting in 2005. An application to retain these items was received from the Department of Chronic Respiratory Disease and Arthritis. Reviews were undertaken by ISDB and comments were received from the WHO Department of Chemical Safety and Médecins Sans Frontières. The Committee noted that as theophylline and aminophylline have limited efﬁcacy in comparison with the other bronchodilators, their relative toxicity becomes a major issue. As noted in the reviews, both products have very narrow therapeutic margins and case reports, case series and studies on theophylline toxicity have been well- documented. One study estimated the overall mortality rate associated with theophylline poisoning to be approximately 10% (6).

9 A Cochrane review (7) indicated that use of intravenous aminophylline in acute asthma did not result in any additional bronchodilatation when compared with standard care, and the frequency of adverse events was higher with aminophylline. In the treatment of exacerbations of chronic obstructive pulmonary disease, the efﬁcacy of methylxanthines was unclear, whereas adverse effects increased signiﬁcantly (8). The Committee recommended that aminophylline and theophylline be deleted from the Model List because of the availability of safer and more effective alternatives on the Model List.

4.1.2 Atropine During its meeting in 2003, the Committee recommended that atropine (as an antispasmodic in the gastrointestinal section) be reviewed for possible fast-track deletion at the meeting in 2005. A review was prepared by the ISDB. The Committee noted that the ISDB review indicated that there had been no systematic review or good clinical trial to support the efficacy of atropine as an antispasmodic. Atropine has a high potential for adverse effects; it offers little help to patients with irritable bowel syndrome and has no proven benefit in diverticular disease or dyspepsia. The Committee therefore recommended that atropine (as an antispasmodic) together with the whole section on antispasmodic medicines be deleted from the Model List because of lack of evidence of efficacy and safety.

4.1.3 Calcium gluconate During its meeting in 2003, the Committee recommended that calcium gluconate be reviewed for possible fast-track deletion at the meeting in 2005. Calcium gluconate is listed in the Model List in Section 4 (Antidotes and other substances used in poisoning) and in Section 27 (Vitamins and minerals, complementary list) in the form of 100mg/ml in a 10-ml ampoule. A review was received from the ISDB. The ISDB review stated that calcium gluconate injection is important for the treatment of acute hypocalcaemic tetany, and consideration should be given to the inclusion in the Model List of other forms of calcium supplementation both for the treatment of less acute hypocalcaemic tetany and as part of the management of bone diseases such as osteoporosis. A Cochrane review indicates that calcium supplementation alone has a small positive effect on bone density. The data

10 show a trend towards reduction in vertebral fractures, but it is unclear if calcium supplementation reduces the incidence of non-vertebral fractures (9). The Committee recommended that calcium gluconate injection be retained in Section 4 for magnesium sulfate poisoning, and in the complementary list of Section 27 for hypocalcaemia and hypocalcaemic tetany, and that the footnote on fast-track deletion be removed from Section 27. The Committee also recommended that an application for the inclusion on the Model List of oral calcium (plus vitamin D) in the treatment of oesteoporosis be invited for its next meeting, and that a review of the section on antidotes be made together with suggestions for deletion and applications for medicines suggested for addition.

4.1.4 Clonazepam During its meeting in 2003, the Committee recommended that clonazepam be reviewed for possible fast-track deletion at the meeting in 2005. A detailed review was provided by the ISDB. The Committee noted that there was inadequate evidence to support the efficacy of clonazepam in the treatment of myoclonic epilepsy. The ISDB review indicated that valproate is the therapy of first choice. This review also indicated that clonazepam may have a place as a second-line drug for the treatment of refractory myoclonic seizures, but no clinical trial is available to support the retention of this item in the Model List. The Expert Committee recommended that clonazepam be deleted because of the lack of evidence of better efficacy or safety when compared with valproate.

4.1.5 Codeine At its meeting in 2003, the Committee recommended that codeine (as an antimotility medicine in the gastrointestinal section) be reviewed for possible fast-track deletion at the meeting in 2005. A review was undertaken by the ISDB. The Committee noted the ISDB review which indicated that there had been no systematic review or good clinical trial to support the efﬁcacy of codeine in the treatment of diarrhoea. It mentioned that the value of antimotility medicines in the treatment of acute diarrhoea (including traveller’s diarrhoea) was not clear. There had been no systematic reviews of the effects of codeine on the duration and severity of symptoms or of its unwanted effects in acute diarrhoea. There was evidence that it could worsen conditions causing toxic

11 megacolon, prolonging fever (in shigellosis), and in children with Shiga toxin-producing Escherichia coli, causing haemolytic–uraemic syndrome. It was contraindicated in patients with bloody or suspected inﬂammatory diarrhoea. However, the Committee also noted that there was a need for symptomatic treatment of diarrhoea in adults with certain conditions, such as HIV/AIDS. The Committee recommended that the heading of the section be changed to “Antidiarrhoeal (symptomatic) medicines for adults”, and that codeine be retained on the list at this time. A review of this subsection, including the potential beneﬁt of loperamide and diphenoxylate and the dangers of their use in children (10), should be presented at its next meeting, especially taking account of the need for symptomatic treatment of diarrhoea in people with HIV/AIDS. A footnote on possible deletion should be added.

4.1.6 Colchicine During its meeting in 2003, the Committee recommended that colchicine be reviewed for possible fast-track deletion at the meeting in 2005. A detailed review was undertaken by the ISDB. The Committee noted that colchicine is the oldest available treatment for gout, but that there are very few systematic reviews or good clinical trials to prove its efficacy in the treatment of gout. Its useful- ness for treating acute attacks is limited by its dose-dependent toxicity and the therapeutic margin is narrow. Patients often experience gastrointestinal adverse effects such as diarrhoea, before relief of gout symptoms. At high doses, colchicine is bone-marrow suppressive and it cannot be dialysed (11). Rarely, its long-term use can result in myopathy. With the availability of other agents, there is a limited special role for colchicine for treatment of acute attacks. The Com- mittee also noted that colchicine is not cheaper than ibuprofen; it has a Median Agency Price (MAP) of US$ 0.1760/defined daily dosage (DDD) compared with US$ 0.0318/DDD for ibuprofen (12). Colchi- cine has not been procured to any great extent by international suppliers over the last five years. The Committee recommended that colchicine be deleted from the Model List because of its unfavourable benefit–risk ratio when compared with non-steroidal anti-inflammatory drugs (NSAIDs) for most people with gout.

4.1.7 Cromoglycic acid During its meeting in 2003, the Committee recommended that cromoglycic acid be reviewed for possible fast-track deletion at the

12 meeting in 2005. Responses were received from the WHO De- partment of Chronic Respiratory Disease and Arthritis and the Japan Institute of Pharmacovigilance, Osaka. A review was undertaken by the ISDB. The Committee noted that there is inadequate evidence to support the inclusion of cromoglycic acid in the Model List. A Cochrane systematic review of trials involving more than 1000 patients aged up to 18 years indicated no evidence that the efﬁcacy of sodium cromoglycate is greater than that of a placebo (13). The Committee recommended that cromoglycic acid be deleted from the Model List because of the availability of more effective and safer alternatives on the Model List.

4.1.8 Diethyltoluamide During its meeting in 2003, the Committee recommended that diethyltoluamide be reviewed for possible fast-track deletion at the meeting in 2005. Comments were received from Médecins Sans Frontières and the Roll Back Malaria programme of WHO. The Committee noted that there is inadequate evidence to establish the efﬁcacy of diethyltoluamide in preventing malaria. Médecins Sans Frontières indicated that case reports on young children had de- scribed serious adverse effects. The WHO Roll Back Malaria Partner- ship supported the deletion of this item from the Model List, as diethyltoluamide is not on the WHO list of pesticides recommended for use in public health programmes. The Committee therefore recommended that diethyltoluamide be deleted from the Model List.

4.1.9 Ergotamine During its meeting in 2003, the Committee recommended that ergotamine be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB, and support for deletion was received from the Global Campaign to Reduce the Burden of Headache. The Committee noted that the available evidence does not support the use of oral ergotamine in the treatment of acute migraine attack. A meta-analysis of placebo-controlled trials of ergotamine was not able to demonstrate a beneﬁt from treatment with oral ergotamine (14). The Committee recommended that ergotamine be deleted from the Model List because of lack of evidence of efﬁcacy and the availability of effective and safe alternatives. The Committee also recommended

13 that a full application for inclusion of a 5HT1 agonist (triptan) for migraine be submitted at its next meeting in 2007.

4.1.10 Ergometrine During its meeting in 2003, the Committee recommended that ergometrine be reviewed for possible fast-track deletion at the meeting in 2005. Comments were received from the WHO Department of Reproductive Health and Research. A review of the evidence found that there was no robust clinical evidence to establish the effectiveness and safety of ergometrine used alone for active management of labour. A Cochrane review (15) of trials of oxytocin alone showed that it reduced postpartum haemorrhage, and that the combination of ergometrine with oxytocin was slightly superior for this outcome. Maternal side-effects were more frequent in women treated with the combination regimen. There was no clinical trial evidence to support the efﬁcacy and safety of ergometrine used alone or in combination with oxytocin for the treatment of postpartum haemorrhage. The Committee recommended that ergometrine injection for the treatment of acute postpartum haemorrhage be retained on the Model List, mainly due to the potential beneﬁts offered by its different pharmacological action (tonic versus periodic contractions that occur with oxytocin). The Committee also recommended that more clinical studies be performed in this area. The Committee saw no indication for ergometrine tablets and recommended that these be deleted from the Model List.

4.1.11 Ether During its meeting in 2003, the Committee recommended that ether be reviewed for possible fast-track deletion at the meeting in 2005. A detailed review was received from the ISDB and a comment was received from the World Federation of Societies of Anaesthesio- logists (WFSA). The Committee noted that halothane is the medicine of choice rather than ether as regards unwanted effects and it enables better precision in controlling the anaesthetic state. This was supported by the ISDB report which recommended that halothane should be used in preference to ether where cost, training, equipment and patient suscep- tibilities permit. Yet both the ISDB and WFSA suggested that ether be retained on the Model List because of its low cost and relative safety when used by inexperienced staff, in the absence of oxygen, and when patients have contraindications to halothane. The Commit-

14 tee also noted that ether has not been procured to any great extent by the large non-proﬁt international suppliers over the last ﬁve years and that its use is generally declining and limited to rural areas. In addition, ether is an explosive chemical with special storage and transport requirements, which places extra demands on national procurement agencies.

The Committee recommended that ether be deleted from the Model List in view of its cumbersome storage and transport requirements, its declining use and the availability of alternative ﬂuorinated inhalational anaesthetic agents; and that a square box be added to the entry for halothane in the Model List.

4.1.12 Factors VIII and IX concentrates During its meeting in 2003, the Committee recommended that factors VIII and IX concentrates be reviewed for possible fast-track deletion at the meeting in 2005. This decision was based on the fact that haemophilia is a rare disease. An application to retain these items on the Model List was received from the European Plasma Fractiona- tion Association (EPFA), Plasma Protein Therapeutic Association (PPTA), and the World Federation of Hemophilia, with support from a number of individuals as well as haemophilia associations from Argentina, Australia, Dominican Republic, Finland, India, Ireland, People’s Republic of China, Portugal, Sri Lanka, Switzerland, the United Kingdom and the USA.

The Committee noted from the application that the approximate estimated prevalence rate of haemophilia in the USA was between 97 and 205 cases per million in the male population, or approximately 75 cases per million in the total population. There were approximately 0.20–0.26 million males with haemophilia in the People’s Republic of China, and the incidence rate of the disease in India was 1 in 10000 live male births. The application also indicated that the cost of treatment with factor VIII concentrate was approximately US$ 4000 (20000 units × US$ 0.20/unit) per patient per year, and that of treatment with factor IX concentrate was similar.

The Committee noted that factors VIII and IX concentrates are life- saving in the treatment for haemophilia, and that the alternative (cryoprecipitate of whole blood) is less safe and more expensive. In addition, use of the concentrates avoids the risk of acquiring HIV and hepatitis. Another argument was that national blood transfusion services were often built around the production of plasma fractions. However, the Committee also noted that the cost of the treatment is

15 relatively high, and that the prevalence of the disease is very low, suggesting low public health relevance. The Committee recommended that factors VIII and IX concentrates be retained on the Model List, accepting the inherent inconsistency caused by the fact that haemophilia is a rare disease. The Committee also recommended that a policy advisory group on rare diseases be established to determine a more general approach to their management.

4.1.13 Imipenem + cilastatin The public health relevance of imipenem + cilastatin was questioned at the 2003 meeting and this item was proposed for possible deletion. Comment was received from the WHO ofﬁcial responsible for AMR strategy, and numerous letters of support for retention were received from Austria, Eastern European countries, the Russian Federation and Sweden. The ISDB produced an extensive review with an annex on comparative costs. The ISDB review pointed out that this medicine has wide activity against both Gram-negative and Gram-positive organisms as well as anaerobes, but because of its expense when compared with other medicines on the Model List, the reviewers suggested that imipenem + cilastatin be deleted. In a detailed fully referenced response, the company which developed the product suggested that deleting this medicine would limit the choice of medicines available to clinicians to treat life-threatening infections, put increased pressure on cheaper antibacterials to develop resistance and eliminate the drug of choice for treating disease caused by extended spectrum beta-lactamase- producing organisms. In addition imipenem + cilastatin has a good safety record, with more than 20 years of experience. The Committee noted that recent reports have highlighted the threat of antibacterial resistance. The Committee noted the minimal cross- resistance of imipenem + cilastatin with other antibiotics, and that this medicine is now off patent and is becoming more widely available as a generic product. The Committee recommended that imipenem + cilastatin be retained on the complementary list, for the treatment of life-threatening hospital-based infections due to suspected or proven multidrug-resistant infection, and that the existing footnote to that effect should be retained.

16 4.1.14 Isoprenaline During its meeting in 2003, the Committee recommended that isoprenaline be reviewed for possible fast-track deletion at the meeting in 2005. The Committee noted that there was no published evidence to support the efficacy of isoprenaline in the emergency treatment of bradycardia. This was supported by the ISDB review which also concluded that cardiac pacing and other drug therapies provide effective, safer alternatives. The Japan Institute of Pharmacovigilance proposed that isoprenaline be retained because it is needed in the treatment of transient and reversible severe bradycardia where cardiac pacing is unavailable, and in the treatment of beta-blocker overdose. Unfortunately, no data were submitted to support these assertions, and the Committee could not find good clinical studies to support its efficacy and safety. The Committee therefore recommended that isoprenaline be deleted from the Model List because of the lack of evidence and the very limited indications for its use.

4.1.15 Levofloxacin Levofloxacin has been a complementary medicine for the treatment of multi-drug resistant tuberculosis (MDR-TB) since 1999. It was suggested for deletion at the 2003 meeting of the Committee because of concern for the public health relevance of the product. The Stop TB Department had suggested that fluoroquinolones have emerged as an important class of drugs in the treatment of MDR-TB. They suggested that levofloxacin is the treatment of choice for MDR-TB. They quoted from a recent review article (16) which supported their position. The Committee recommended that levofloxacin be retained as a complementary medicine for the treatment of MDR-TB, and the footnote signalling the restriction of use for this specific indication be retained. The Committee did not recommend the use of a square box symbol to encompass both levofloxacin and ofloxacin, as this might be taken to include gatifloxacin or moxifloxacin for which no review has been undertaken. The Committee also recommended that the evidence for all medicines for the treatment of MDR-TB be reviewed at its next meeting, in the light of increasing experience with their use.

17 4.1.16 Local anaesthetic, astringent or anti-inflammatory as antihaemorrhoidal medicines During its meeting in 2003, the Committee recommended that antihaemorrhoidal medicines be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB. The Committee noted that there is no strong evidence to support the efficacy of topical products containing local anaesthetics, astringents or anti-inflammatory medicines in the treatment of haemorrhoids, as was also concluded in the ISDB review. Therefore the Committee recommended that antihaemorrhoidal medicines (ointment or suppository) and the section on antihaemorrhoidal medicines be deleted from the Model List because of lack of evidence of efficacy and safety, and because of uncertainty as to the real burden of disease caused by this condition.

4.1.17 Medroxyprogesterone acetate (depot injection 150mg/ml) During its meeting in 2003, the Committee recommended that medroxyprogesterone acetate (depot injection 150mg/ml) be reviewed for possible fast-track deletion at the meeting in 2005. Com- ments in support of retention were received from the WHO Department of Reproductive Health and Research, Médecins Sans Frontières and the Expert Committee on the Essential Drugs List of Sri Lanka. The Committee noted that medroxyprogesterone acetate depot injection (DMPA) is the only three-monthly injectable contraceptive currently available and widely used in developing countries, and that the efficacy of this item has been reviewed and is well-documented. It was reported that the risk of unintended pregnancy during the first year of usage was 3% among typical users and 0.3% among perfect users (17). The applicant suggested that DMPA be upgraded from the complementary to the core list. However, the Committee also noted that this medicine has been reported to reduce bone density in comparison with estrogens, but the long-term overall clinical implications of this finding have not yet been determined. The Committee noted that there is no alternative three-monthly injectable contraceptive. While noting the safety concerns, the Committee recommended that DMPA be retained on the Model List, moved from the complementary list to the core list as requested by the WHO Department of Reproductive Health and Research, and that the footnote on possible fast-track deletion be removed.

18 4.1.18 Medroxyprogesterone acetate (tablet 5mg) During its meeting in 2003 medroxyprogesterone acetate (MPA) tablet, 5mg, was marked for possible fast-track deletion of the meeting in 2005, due to the concerns about adverse effects, including risk of decreased bone mineral density (BMD). A review was carried out that evaluated negative effects of oral formulations of MPA on BMD, as well as clinical outcomes such as fractures.

The Committee noted that the MPA 5-mg tablet is generally used for short-term treatment of dysfunctional metrorrhagia and endometrio- sis. The review of effects on BMD suggested that only long-term use of MPA may be associated with signiﬁcant changes in BMD and therefore the Committee decided to retain this product on the Model List at this time. However, the Committee recommended that a further review on the efﬁcacy, safety and public health relevance of norethisterone, medroxyprogesterone acetate and also of ethinylestradiol be presented at its next meeting, and that a footnote to this effect be added in the Model List.

4.1.19 Nalidixic acid During its meeting in 2003 the Committee recommended that nalidixic acid be reviewed for possible fast-track deletion at the meeting in 2005. Reviews were received from the ISDB and Médecins Sans Frontières, and a comment was received from the WHO Department of Child and Adolescent Health and Development, all supporting the deletion of this item from the Model List.

The Committee noted that there was no strong evidence on the efficacy of nalidixic acid in the treatment of urinary tract infections. Both ISDB and Médecins Sans Frontières indicated that antibacterial resistance to nalidixic acid developed quickly, and this may induce resistance to other quinolones such as ciprofloxacin (18). The WHO Department of Child and Adolescent Health and Development stated that ciprofloxacin is now the recommended first-line antibiotic for treating shigellosis, and that the use of nalidixic acid should be discontinued even in areas where it is still effective against Shigella (19). The Committee also noted that the cost/DDD of nalidixic acid is higher than that of ciprofloxacin (MSP US$ 0.3488 and MAP US$ 0.4488 for nalidixic acid versus MSP US$ 0.0618 and MAP US $0.0890 for ciprofloxacin) (12).

The Committee recommended that nalidixic acid be deleted from the Model List because of lack of evidence of efﬁcacy in current practice and the availability of better alternatives.

19 4.1.20 Niclosamide During its meeting in 2003, the Committee recommended that niclosamide be reviewed for possible fast-track deletion at the meeting in 2005. Submissions supporting the retention of niclosamide were received from the WHO Department of Communicable Diseases, Surveillance and Response.

The Committee noted that niclosamide is effective for the treatment of cestode infections. It was estimated that in Latin America 75 million people live in areas where cysticercosis is endemic and approximately 400000 people have symptomatic disease (20). Niclosamide is not absorbed from the gastrointestinal tract.

A review sponsored by the WHO Quality Assurance and Safety of Medicines team conﬁrmed that no major safety concerns have been raised in relation to the use of this item. Niclosamide is not contraindicated in children and pregnant women. Its efﬁcacy and safety in treating Taenia solium carriers in the presence of (neuro) cysticercosis has an advantage over praziquantel because it does not increase the likelihood of seizures.

The Committee recommended that niclosamide be retained on the Model List as a reserve medicine, and also for treatment of patients in endemic areas presenting with epileptic seizures which could be caused by cysticercosis and in whom the use of praziquantel is not possible.

4.1.21 Nifedipine During its meeting in 2003, the Committee recommended that long- acting nifedipine be reviewed for possible fast-track deletion at the meeting in 2005. A review was prepared by the WHO Collaborating Centre for Research and Training in Pharmaco-epidemiology in Barcelona, Spain, and comments were received from Médecins Sans Frontières.

The Committee noted that the presentation of nifedipine in the 13th Model List was slightly ambiguous and confirmed that only slow- release tablets of 10mg were listed. The Committee also noted that short-acting nifedipine is not recommended in the treatment of hypertension due to its relative lack of safety when compared with other antihypertensive medicines. The review prepared by the Collaborating Centre identified that the clinical trial evidence show- ing benefits of dihydropyridine calcium-channel blockers was strongest for amlodipine.

20 On the basis of the review, the Committee recommended that sustained-release nifedipine be replaced with amlodipine (5mg tablet) with a square box as the representative long-acting dihydropyridine calcium channel blocker. The Committee also recommended a review of the continued use of the square box at its next meeting.

4.1.22 Oxamniquine During its meeting in 2003, the Committee recommended that oxamniquine be reviewed for possible fast-track deletion at the meeting in 2005. Submissions recommending the retention of oxamniquine were received from the WHO Department of Communicable Diseases, Surveillance and Response. A review sponsored by the WHO Quality Assurance and Safety of Medicines team conﬁrmed that no major safety concerns have been raised in relation to the use of this item. The Committee noted that although praziquantel is the medicine of choice for treating Schistosomiasis mansoni, oxamniquine can be used in cases when praziquantel may be contraindicated or in the case of resistance. A Cochrane review reported that oxamniquine has equal efﬁcacy to praziquantel in the treatment of S. mansoni although lower doses of oxamniquine (<30mg/kg) may not be as effective in some areas (21). The safety review reported a relatively high incidence of minor gastrointestinal and central nervous system side-effects, but these have not limited its widespread use. Oxamniquine is generally more expensive than praziquantel. Despite some of the comparative disadvantages mentioned above, the Committee recommended that oxamniquine be maintained on the Model List for use in case of failure of treatment with praziquantel.

4.1.23 Polygeline In 2003 the Expert Committee recommended reviewing polygeline for possible fast-track deletion at the meeting in 2005. One review was received from the ISDB and one from Médecins Sans Frontières. A Cochrane review (22) of 57 trials involving 3659 patients compared the effects of different colloid solutions in patients thought to need blood volume replacement. It showed that there is no evidence that one colloid solution is more effective or safer than any other. Another Cochrane review (23) indicated that there is no evidence from randomized controlled trials that resuscitation with colloids, compared with resuscitation with crystalloids, reduces the risk of death in patients with trauma or burns or following surgery. The Committee also

21 noted that the cost of polygeline (US$ 0.0126/ml) is twice that of dextran 70 in normal saline (US$ 0.0056/ml) (12). The Committee concluded that polygeline and dextran 70 are similar in safety and efﬁcacy. The Committee decided that, in view of its lower price, dextran 70 should be retained on the Model List, with a square box to cover polygeline. The choice made will depend on national circumstances. A full review of colloids compared with crystalloids would be welcome at the next meeting of the Committee.

4.1.24 Procainamide During its meeting in 2003, the Committee recommended that procainamide be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB. The Committee noted that there is evidence that calls into question the continued use of procainamide in the treatment of arrhythmias. However, because of the limited choice of antiarrhythmics available on the current Model List, the Committee recommended that procainamide be retained on the Model List at this time, that the subsection of antiarrhythmic medicines (12.2) be fully reviewed at the next meeting of the Expert Committee in 2007, including full applications for amiodarone and sotalol, and that a footnote be added to this effect.

4.1.25 Pyrantel During its meeting in 2003, the Committee recommended that pyrantel be reviewed for possible fast-track deletion at the meeting in 2005. Submissions recommending the retention of pyrantel were received from the WHO Department of Communicable Disease Surveillance and Response. A comprehensive safety review was also prepared. The Committee noted that, in adults, pyrantel was equally effective and as safe as the benzimidazoles, but that a previous price advantage no longer existed as benzimidazoles were now generally cheaper. Whereas benzimidazoles are therefore the medicines of choice for treating nematode infections, pyrantel can still be used when benzimidazoles are contraindicated, as in the case of resistance, or in the treatment of children under one year old (24), although the latter need is rare. The Committee recommended that pyrantel be retained on the Model List as an alternative to benzimidazoles. At country level the choice between the two medicines would depend on the local cost.

22 4.1.26 Quinidine During its meeting in 2003, the Committee recommended that quinidine be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB. The Committee noted that there is evidence that calls into question the continued use of quinidine in the treatment of arrhythmias. It was reported that quinidine was effective in the treatment of atrial ﬁbril- lation or sustained ventricular arrhythmias. Due to the limited choices of anti-arrhythmics available on the current Model List, the Commit- tee recommended that quinidine be retained on the List at this time, that the subsection of anti-arrhythmic medicines (12.2) be fully reviewed at the next meeting of the Expert Committee in 2007, including full applications for amiodarone and sotalol and that a footnote should be added to this effect.

4.1.27 Salbutamol During its meeting in 2003, the Committee recommended that salbutamol (as a tocolytic) be reviewed for possible fast-track deletion at the meeting in 2005. Comments were received from the WHO Department of Reproductive Health and Research, Médecins Sans Frontières and BMJ-Clinical Evidence. The Committee noted that there is inadequate evidence to support the efficacy of salbutamol as a tocolytic agent. No systematic review is available relating to salbutamol specifically, but a Cochrane review concluded that terbutaline is ineffective as a tocolytic (25). Betamimetics are effective in facilitating external cephalic version, but one small randomized controlled trial showed that salbutamol did not significantly reduce failed cephalic version. There is also inadequate evidence to support the use of betamimetics in impaired fetal growth, placenta praevia and fetal distress. The Committee therefore recommended that salbutamol (as a tocolytic) be deleted from the Model List.

4.1.28 Silver nitrate eye solution During its meeting in 2003, the Committee recommended that silver nitrate eye solution be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB, and a comment was received from the WHO Department of Chronic Diseases, Prevention and Management. The Committee noted that there was inadequate evidence on the safety of silver nitrate eye solution in the prevention of neonatal

23 gonococcal conjunctivitis. The ISDB and the WHO Department of Chronic Diseases, Prevention and Management both raised safety concerns and supported the deletion of this item from the Model List. The aqueous solutions had caused chemical conjunctivitis due to the evaporation of the solvent over time, especially in tropical conditions, and such conjunctival irritation hampered eye contact of the neonate with the mother, which was claimed to hinder bonding. The Com- mittee also noted that tetracycline ointment, which is already in the Model List, can be used for the same indications with fewer unwanted effects. The Committee therefore recommended that silver nitrate eye solution be deleted from the Model List.

4.1.29 Sodium fluoride During its meeting in 2003, the Committee recommended that sodium fluoride (in any appropriate formulation) be reviewed for possible fast-track deletion at the meeting in 2005. Responses were received from the WHO Oral Health Programme and the World Dental Federation which argued for the retention of sodium fluoride on the Model List. Comments on safety issues were received from Fluoride Action Network and Medwatcher, Japan. The Committee also received a review by the ISDB on this item. The Committee noted that the efficacy of topical fluoride formulations in preventing dental caries is firmly established (26–30). The Committee also noted that the selection of a suitable preparation should take into account local circumstances, including the fluoride content of drinking-water. Fluoride tablets are no longer recommended because of the risk of fluorosis when they are used in excess. The Committee therefore recommended that sodium fluoride be retained on the Model List, but that the description be changed to “in any appropriate topical formulation”, and that the square box and the footnote regarding fast-track deletion be removed.

4.1.30 Spectinomycin During its meeting in 2003, the Committee recommended that spectinomycin be reviewed for possible fast-track deletion at the meeting in 2005. A response was received from the WHO Depart- ment of Reproductive Health and Research, and reviews were received from Médecins Sans Frontières and the ISDB. All responses argued for the retention of spectinomycin on the Model List. Spectinomycin was recommended in the WHO Guidelines for the management of sexually transmitted infections (31) as one of the

24 ﬁrst-line treatment options for uncomplicated ano-genital gonococcal infections, disseminated gonococcal infection, adult gonococcal conjunctivitis and pelvic inﬂammatory disease. The Committee noted that spectinomycin can be used in patients who are intolerant to cefalosporins or quinolones. The Committee recommended that spectinomycin continue to be listed in the WHO Model List, as an alternative to cephalosporins in the treatment of gonorrhoea and chancroid in adults.

4.1.31 Sun protection agents During its meeting in 2003, the Committee recommended that sun protection agents be reviewed for possible fast-track deletion at the meeting in 2005. A review was received from the ISDB. The Committee noted that the use of topical sun protection agents (sunscreen products) containing substances that protect the skin against ultraviolet radiation (UVA and UVB) prevents squamous- cell skin cancer in susceptible people (32). The Committee also noted that although the public health relevance of this item for the prevention of skin cancer is high, sunscreens are normally not provided by public facilities and that provision through such sources was not needed. The Committee therefore recommended that topical sun protection agents be deleted from the Model List.

4.1.32 Thioacetazone + isoniazid Thioacetazone in combination with isoniazid has been a complementary medicine since 1990. It was suggested for possible fast-track deletion by the Committee at its meeting in 2003 because of concern for the public health relevance of thioacetazone. The WHO Stop TB Department undertook a comprehensive review of the use of this medicine and the attitudes of the world’s major TB service providers. Comments were received from the Damien Foundation, the Interna- tional Union against Tuberculosis and Lung Disease (IUATLD), the Deutsche Lepra- und Tuberkulosehilfe e.V. (DAHW), the Centers for Disease Control, USA (CDC) and Médecins Sans Frontières. Thioacetazone has been used in combination with isoniazid for the treatment of tuberculosis since the 1960s, to prevent the development of resistance to isoniazid. Thioacetazone has always been associated with adverse cutaneous reactions. However, if a patient is co-infected with HIV, the frequency and severity of these reactions is increased, sometimes leading to death. As a result the use of thioacetazone in

25 HIV-positive patients has been discouraged. Ethambutol and rifampicin are effective alternatives to thioacetazone (33–35). In a sur- vey undertaken by the Stop TB Department, thioacetazone was being used in only seven countries, and in many of these its use was being phased out. These countries carry 1.5% of the global TB burden. Of the agencies that responded to queries about the position of the medicine, support for retention was very mixed. CDC suggested that the risks outweigh the benefits; DAHW strongly suggested removing the product from the Model List. Conversely, the IUATLD supported its retention on the basis of safety for category 1 patients, low price, and concern that in view of the limited number of products available to treat TB, losing one of them would be a serious matter. The Damien Foundation supported retention based on their experience of using this medicine in Bangladesh. Médecins Sans Frontières suggested that thioacetazone be retained for the treatment of pregnant women who are HIV-negative and who require retreatment. In terms of comparative cost-effectiveness, thioacetazone + isoniazid costs US$ 1.24 to US$ 1.71 as compared with a cost of US$ 2.93 (MAP) per person for isoniazid + ethambutol. This costing does not take into account the cost of HIV testing and counselling to preclude the presence of HIV. The conclusion of the WHO Stop TB Department was to recommend keeping thioacetazone + isoniazid on the complementary list of the Model List for the next two years pending further assessment. This was on the grounds that this medicine continues to be used in a few Member States and because of its potential in prevention of emergence of resistance. However, the Stop TB Department recommended adding a box, after the text on thioacetazone + isoniazid in the Model List and the WHO model formulary, containing the following note: Thioacetazone may be used only where HIV-infection has been excluded because of the risk of serious skin reactions. While giving due weight to the proposal by the Stop TB Department and the suggestions from IUATLD, Médecins Sans Frontières and the Damien Foundation, the Committee recommended that thioacetazone + isoniazid be removed from the Model List because it does not fulfil the definition of a complementary product. It cannot be considered as needing specialized diagnostic or monitoring facilities, and/or specialist medical care, and/or specialist training. In addition, the strong association of HIV with TB means that all patients being considered for treatment with thioacetazone should receive HIV testing, which makes thioacetazone + isoniazid less cost-effective than

26 alternative products such as isoniazid + ethambutol or rifampicin + isoniazid. Removing thioacetazone + isoniazid from the Model List does not preclude individual countries or programmes continuing to use the combination nor does it preclude returning the combination to the Model List if changing needs in relation to the treatment of MDR-TB require it.

4.1.33 Triclabendazole During its meeting in 2003, the Committee recommended that triclabendazole be reviewed for possible fast-track deletion at the meeting in 2005. Submissions recommending the retention of triclabendazole were received from the WHO Department of Commu- nicable Disease Surveillance and Response. A comprehensive safety review was also considered. The Committee noted that approximately 2.5 million people worldwide are affected by fascioliasis. Triclabendazole is more efficacious than praziquantel in treating paragonimiasis but it is also more expensive (12). There are also reports of the successful use of triclabendazole in treating praziquantel-ineffective fascioliasis. A review sponsored by the WHO Quality Assurance and Safety of Medi- cines team confirmed that triclabendazole appears to be very well tolerated; fewer side-effects were recorded when triclabendazole was used than when praziquantel was used. The small number of reports in the WHO database could be a reflection of its safety, though lack of pharmacovigilance systems in several of the countries where the medicine is used may also be a factor. In view of the above information the Committee recommended that triclabendazole be retained on the Model List, as the medicine of choice for treatment of fascioliasis and paragonimiasis.

4.2 Applications for additions 4.2.1 Caffeine citrate An application was submitted by the Royal Children’s Hospital, Melbourne, Australia, with the support of the WHO Department of Child and Adolescent Health and Development, for the inclusion in the Model List of caffeine citrate, oral solution 20mg/ml, and IV injection 20g/ml, for the treatment of apnoea of prematurity in neonates, as an example of the therapeutic class of methylxanthines, with the alternatives being aminophylline and theophylline. The Committee noted that evidence is available to support the efﬁ- cacy of caffeine citrate in the treatment of apnoea in preterm neonates. Reviews (36) indicated that caffeine appears to have similar

27 short-term effects on apnoea/bradycardia, with fewer cardiovascular adverse effects than theophylline. However, there are insufﬁcient data to evaluate adequately the side-effects and no data to determine its effects in different gestational age groups. Reviews also indicated that the safety of therapy with methylxanthines was uncertain, especially regarding long-term growth and development. The Committee noted that caffeine is considerably more expensive than theophylline and that the evidence on the effectiveness and safety of methylxanthines in the treatment of apnoea in preterm neonates is not robust because the number of trials and patients is limited. The Committee noted that a large clinical trial is about to be completed and therefore decided to defer its decision until its next meeting pending the outcome of this trial.

4.2.2 Cefixime An application was received from the WHO Department of Reproductive Health and Research, Controlling Sexually Transmit- ted and Reproductive Tract Infections team, to include cefixime, oral tablet 400mg, for the treatment of uncomplicated gonorrhoea infection. The Committee noted that cefixime is well tolerated and that most adverse drug reactions are related to the gastrointestinal system. The costs of single dose oral cefixime and ceftriaxone injection are comparable. Cefixime is listed in the WHO Guidelines for the management of sexually transmitted infections (31) and the European Sexually Transmitted Disease Guidelines as one of the recommended options. However, the Committee also noted that concerns have been raised about the emerging resistance of Neisseria gonorrhoeae (37). The Committee recommended that cefixime be added to the Model List for the treatment of uncomplicated ano-genital gonorrhoea only, and the addition of a footnote to that effect.

4.2.3 Clotrimazole An application was received from UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction, the WHO Department of Repro- ductive Health and Research and BMJ Knowledge, BMJ Publishing Group, London, England, to include clotrimazole (1% and 10% vaginal creams, and 100mg and 500mg vaginal tablets) for the treatment of uncomplicated candidiasis.

28 The Committee noted that there has been adequate clinical evidence to support the efficacy and safety of topical and intravaginal clotrimazole in the treatment of vulvovaginal candidiasis. The efficacy of clotrimazole in uncomplicated candidiasis in non-pregnant women was demonstrated by four clinical trials comparing clotrimazole with placebo (38). A Cochrane review (39), based on five trials, indicated that imidazole drugs were clearly more effective than nystatin in treating vaginal candidiasis in pregnancy. Topical administration of clotrimazole is recommended by Médecins Sans Frontières and in the WHO Guidelines for the management of sexually transmitted diseases (31). The Committee therefore recommended that clotrimazole (1%, 10% vaginal cream; 100mg, 500mg vaginal tablets) be included in the Model List for the treatment of vulvovaginal candidiasis.

4.2.4 Combination injectable contraceptives With the support of the Geneva Foundation for Medical Education and Research, an application was submitted by UNDP/UNFPA/ WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction and the WHO Department of Reproductive Health and Research, to include two combination injectable contraceptives, medroxyprogesterone acetate + 25mg estradiol cypionate 5mg (MPA/E2C) and norethisterone + enanthate 50mg estradiol valerate 5mg (NET-EN/E2V) on the Model List. The Committee also noted the information contained in a new Cochrane review which is in press (40). The evidence provided to the Committee showed that the efﬁcacy of combination injectable contraceptives (CICs) for contraception was equivalent to that of progestogen-only and combined oral contraceptives. The Committee noted that CICs had some advantages in relation to more regular bleeding patterns and convenience of use, but there was a lack of data on long-term safety. Although the Committee recognized the drive towards greater patient choice of contraceptives, it also questioned the public health need for this preparation in view of the lack of compelling evidence of better efﬁcacy, convenience and safety. The Committee therefore recommended that the application be rejected.

4.2.5 Emtricitabine Emtricitabine had been proposed for addition to the list of antiretroviral products by the company developing the product. This medicine was approved by the US Food and Drug Administration on

29 2 July 2003 and in Europe on 24 October 2003. A full application was submitted. A report on safety was submitted by the WHO Advisory Committee on Safety of Medicinal Products. The reviewer noted that most of the data provided were unpublished study reports from the sponsor or papers available in abstract only. Most were cited as poster publications only and these data could not be independently evaluated. In addition the safety data appeared to be based on a limited number of patients participating in the efﬁcacy trials. The WHO Advisory Committee on Safety of Medicinal Prod- ucts noted that use of emtricitabine had been low and therefore limited safety data were available. They expressed concern about the acceptability and tolerability of adverse effects. The Committee noted that it could not make a recommendation to include a medicine on the Model List on the basis of data which could not be made publicly available afterwards. The Committee therefore decided to defer its decision because of the lack of publicly available data that would allow for an independent assessment of comparative effectiveness and safety in populations likely to use the medicine.

4.2.6 Emtricitabine + tenofovir fixed-dose combination Emtricitabine + tenofovir had been proposed as a fixed-dose combination for addition to the list of antiretroviral products by the company developing the medicine. The company had also submitted applications for the individual components to be added to the list. The Committee noted that the fixed-dose combination had only recently been approved by the US Food and Drug Administration, but that it is increasingly being used in national programmes. However, it would be illogical to consider the combination so long as the individual medicines had not been added to the Model List. The Commit- tee concluded that listing of the combination at this stage would be premature, and decided to defer its decision because of the lack of information, for example, in comparison with lamivudine.

4.2.7 Etonogestrel-releasing implant An application was submitted by UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Train- ing in Human Reproduction and the WHO Department of Reproduc- tive Health and Research, with support from the Geneva Foundation for Medical Education and Research, to include etonogestrel- releasing implant as a contraceptive on the Model List. The Committee noted that etonogestrel is an effective and safe contraceptive. However, it also noted that the insertion of the implant

30 should be undertaken only by specially trained personnel, and that the nature of removal depends on the correctness of the implant insertion. Etonogestrel implant was expensive. The Committee recognized the potential value of an implantable progestogen. The advantages were the clear evidence of efficacy, the prolonged effect, and therefore the suitability for women wanting long periods of protection. The disadvantages noted were the difficul- ties associated with insertion and, especially with removal, and the training required for this purpose, and the relatively high acquisition cost. After consideration of the balance of benefits, harms, suitability, and the need for the additional choice and the relatively high cost, the Committee decided to reject the application.

4.2.8 Ibuprofen paediatric suspension An application for the inclusion of ibuprofen paediatric suspension 20mg/ml on the Model List was reviewed by the Expert Committee at its meeting in 2003. The Committee rejected that application on the basis that there was insufficient evidence to conclude that ibuprofen provides an antipyretic effect superior to that of paracetamol, and because data on the comparative safety and cost-effectiveness of ibuprofen and paracetamol were lacking. A full application was submitted to the Expert Committee in 2005 by the International Ibuprofen Foundation (IIF), Marlborough, England, with support from Boots Healthcare International, Wyeth Consumer Health, and several clinicians from Australia, the Netherlands, the United Kingdom and the USA. A detailed review was provided by the Cochrane Pain and Palliative Care Group. The WHO Department of Child and Adolescent Health and Development recommended rejection of the application. The Committee noted that ibuprofen has comparable efficacy to paracetamol in reducing body temperature. However, paracetamol is safer. A randomized controlled study involving 27065 febrile children confirmed this view (41). The Committee also noted that ibuprofen is more expensive than paracetamol; the MAP of ibuprofen is US$ 0.0105/ml and that for paracetamol syrup US$ 0.0008– 0.0032/ml (12). The Committee recommended that ibuprofen paediatric suspension not be added to the Model List in view of its unfavourable benefit– risk ratio when compared to paracetamol, and its higher cost. The Committee also recommended that no further application be considered without substantial new data.

31 4.2.9 Levonorgestrel-releasing implant An application was submitted by the United Nations Development Programme/United Nations Population Fund (UNDP/UNFPA)/ WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction and the WHO De- partment of Reproductive Health and Research, with support from the Geneva Foundation for Medical Education and Research, to include levonorgestrel-releasing implant as a contraceptive on the Model List. The Committee noted that levonorgestrel is an effective and safe contraceptive. However, it also noted that the insertion of the implant should be undertaken only by specially trained personnel, and that the nature of removal depends on the correctness of the implant insertion. Levonorgestrel implant was expensive. The Committee recognized the potential value of an implantable progestogen. The advantages were the clear evidence of efficacy, the prolonged effect, and therefore the suitability for women wanting long periods of protection. The disadvantages noted were the difficul- ties associated with insertion, and especially with removal, and the training required for this purpose, and the relatively high acquisition cost. After consideration of the balance of benefits, harms, suitability, and the need for the additional choice and the relatively high cost, the Committee decided to reject the application.

4.2.10 Levonorgestrel-releasing IUD An application was submitted by the UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction and the WHO Department of Reproductive Health and Research, with support from the Geneva Foundation for Medical Education and Research, to include levonorgestrel-releasing IUD as a contraceptive on the Model List. The Committee noted that levonorgestrel-releasing IUD (LNG-20 IUD) is an effective contraceptive. The results of a Cochrane review (42) indicated that LNG-20 IUD is as effective as non-hormonal IUDs > 250mm2. However its discontinuation rate is signiﬁcantly higher than that of copper IUDs, with amenorrhoea as the main reason given for discontinuing use of LNG-20 IUD. The Committee also noted that LNG-20 IUD is more expensive than copper IUDs. The Committee recommended rejection of the application for inclusion of the levonorgestrel-releasing IUD for contraception because of

32 the lack of evidence for better efﬁcacy, its higher discontinuation rate and because it is more expensive than the copper IUD already in the Model List.

4.2.11 Methadone and buprenorphine An application was received from the WHO Department of Mental Health and Substance Abuse and Department of HIV/AIDS with support from the WHO Collaborating Center/College on Problems of Drug Dependence, Philadelphia, Virginia Commonwealth University Institute for Drug and Alcohol Studies, Alcohol and other Drugs Control of Australia, European AIDS Treatment Group, Central and Eastern European Harm Reduction Network, and more than 10 individuals and other organizations. Comment was received from the Islamic Republic of Iran. The Committee noted that the most widely used illicit opioid is heroin, mainly through intravenous injecting. It is estimated that there are 12.6 million injecting drug users (IDUs) worldwide, approximately 10% of HIV infections are associated with injecting drug use. Intravenous drug users are also at a high risk of exposure to hepatitis B and C. Treatment of heroin dependence is therefore of high public health relevance. Both buprenorphine and methadone are effective for the treatment of heroin dependence (43, 44). However, methadone maintenance therapy at appropriate doses is the most effective in retaining patients in treatment and suppressing heroin use (45). Methadone is less costly than buprenorphine. It was reported that the cost of buprenorphine per patient per year varied from US$ 300–600 for the generic product to approximately US$ 1750– 3500 for a branded product in India. The cost of methadone per patient per year in developing countries was reported as US$ 29 for the Slovak Republic, US$ 60 as a generic product from the Netherlands and US$ 180 in the Islamic Republic of Iran. The Com- mittee also noted that misuse of buprenorphine by IDUs is reported from the Islamic Republic of Iran. The Committee noted that the quality of the data will be inherently weaker than in other therapeutic areas because of the type of disorder and the situations in which it occurs. In addition to conventional randomized controlled trials with abstinence rate as an outcome, the evidence of effectiveness in various societal effects (such as a reduction in criminality) should also be taken into consideration. The Committee noted evidence that the use of methadone reduces seroconversion of HIV/AIDS (46). It has also been noted that methadone interacts with antiretroviral medicines, but that this only affects the serum level of methadone, which needs to be adjusted according

33 to the patient response. The Committee noted that there is less clinical experience with buprenorphine than with methadone, but that there is more pharmacological evidence and evidence of favourable societal outcomes. The Committee recommended that the treatment should be initiated and monitored by specially trained staff within an established support structure, but recognized that this would not necessarily require a tertiary hospital setting.

The Committee recommended that methadone (oral solution 5mg/ 5ml, 10mg/5ml; or concentrate for oral solution 5mg/ml, 10mg/ml) be added to the complementary list of the Model List, with a square box to cover buprenorphine only, within a new subsection “Medicines used in substance dependence programmes” and that a footnote be added that these products should be used only within an established programme.

4.2.12 Methoxyﬂurane An application was received from Medical Development Interna- tional Ltd, Springvale, Australia, to include methoxyﬂurane, inhaled 3-ml preparation (Penthrox® Inhaler), as an example of preoperative medication and sedation for short-term procedures, and as an analgesic (section 2).

The Committee noted that there was inadequate evidence to support the inclusion of methoxyflurane on the Model List, either for analgesia or for short-term anaesthesia. A list of 12 randomized clinical studies (conducted between 1966 and 1975) and two more recent studies (conducted in 2002) was provided in the application, mostly conducted with small numbers of patients. It was reported that a study involving 1257 women in labour (47) indicated that methoxyflurane had equal analgesic effect to trichloroethylene and nitrous oxide, and another study involving 1616 women in labour (48) indicated that methoxyflurane provided an analgesic effect equal to that of nitrous oxide and cyclopropane. However, no detailed information on the methodology of the trials was provided. No compelling evidence was provided to show that, in clinical practice, methoxyflurane is more efficacious or safer than the alternative. Concern about its efficacy and safety was further heightened by the fact that it is registered in only two countries despite having been available for over 30 years.

The Committee recommended that methoxyﬂurane not be added to the Model List in view of the lack of evidence that it is more efﬁca- cious or safer than its alternatives.

34 4.2.13 Miltefosine An application was received from the manufacturer to include miltefosine 10mg and 50mg capsules for the treatment of leishmaniasis. Comments on safety were received from Médecins Sans Frontières and the Department of Communicable Disease Surveil- lance and Response. The Committee recognized the importance of encouraging applications for medicines for neglected diseases. The Committee noted that oral miltefosine shows equal efficacy to amphotericin B in the treatment of visceral leishmaniasis in adults (49). However, the observa- tion that many patients discontinued miltefosine due to adverse reactions indicates that more data need to be generated about its safety, especially keeping in mind the risk of teratogenicity. Very little is known about the pharmacokinetic profile of miltefosine in humans, and the dosage schedule for adults with visceral leishmaniasis is not very clear. The Committee also noted that miltefosine is registered in India (in 2002) only for the treatment of visceral leishmaniasis, and its availability is restricted. In addition, miltefosine has not been suffi- ciently tested for treatment of cutaneous leishmaniasis. The Committee considered that miltefosine may be of potential value for the treatment of visceral leishmaniasis. However, from the evidence currently available, the Committee recommended rejection of the application for miltefosine. Any future application should include data demonstrating comparative effectiveness, including for cutaneous leishmaniasis; evidence for safety particularly in relation to the question of teratogenicity; and an evaluation of the comparative cost-effectiveness, including in comparison with liposomal amphotericin B.

4.2.14 Nifedipine During its meeting in 2003, the Committee recommended that long- acting nifedipine be reviewed for possible fast-track deletion at the meeting in 2005. A review was prepared by the WHO Collaborating Centre for Research and Training in Pharmacoepidemiology in Barcelona, Spain, and comments were received from Médecins Sans Frontières. The Committee noted that the presentation of nifedipine in the 13th Model List was slightly ambiguous and conﬁrmed that only slow release tablets of 10mg were listed. The Committee also noted that short-acting nifedipine is not recommended in the treatment of hypertension due to its relative lack of safety when compared with other antihypertensive medicines. The review prepared by the

35 Collaborating Centre identiﬁed that the clinical trial evidence show- ing beneﬁts of dihydropyridine calcium-channel blockers was strongest for amlodipine. Based on the review, the Committee recommended that sustained- release nifedipine be replaced with amlodipine (5mg tablet) with a square box as the representative long-acting dihydropyridine calcium channel blocker. The Committee also recommended a review of the continued use of the square box at its next meeting.

4.2.15 Mifepristone with misoprostol An application was received from the UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP), the WHO Department of Reproductive Health and Research and the Geneva Foundation for Medical Education and Research to include in the Model List sequential administration of oral mifepristone and intravaginal misoprostol for induction of medical abortion. The Committee noted a Cochrane review of 39 trials (50) which showed that sequential administration of a single-dose mifepristone oral 200-mg tablet followed by a vaginal single dose of misoprostol, 800 micrograms in 36 to 48 hours is effective, safe and convenient in inducing medical abortion until nine weeks of pregnancy. Major com- plications appeared to be rare, the most common complication being the need for blood transfusion (about 0.2%). It was reported that the side-effects (nausea, vomiting and diarrhoea) were mainly due to prostaglandins. Higher doses were associated with increased incidence of side-effects. The risks of bleeding, abdominal pain, fever and dizziness in the medical abortion population were higher than those in the surgical abortion population (51). In addition, the duration of bleeding caused by medical abortion was longer than that caused by surgical abortion. The Committee noted from the application that the mifepristone/ misoprostol regimen for medical abortion in the ﬁrst nine weeks of pregnancy has been registered in the following countries in Europe: Austria, Belgium, Finland, France, Germany, Greece, Luxembourg, the Netherlands, Norway, Romania, Spain, Sweden, Switzerland and the United Kingdom. The regimen has also been registered in Azerbaijan, Georgia, India, Israel, New Zealand, the People’s Re- public of China, the Russian Federation, South Africa, Tunisia, Ukraine, the USA, Uzbekistan and Viet Nam. The Committee noted that the use of this medication in medical abortion should be undertaken under close medical supervision, and

36 that its efﬁcacy decreases if used after nine weeks of gestation. The Committee therefore recommended that mifepristone (200-mg tablet) followed by misoprostol (200-microgram tablet) be included on the complementary list of the Model List for medical abortion within nine weeks of the start of pregnancy, and that the following footnote be added: Requires close medical supervision. Note from the Secretariat: In reviewing the recommendation relating to this combination of products, the Director-General decided to add a note adjacent to the combination in the WHO Model List stating: Where permitted under national law and where culturally acceptable.

4.2.16 Misoprostol, low dose An application was received from the UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction, the WHO Department of Repro- ductive Health and Research and BMJ Knowledge, to include misoprostol, 25–50-microgram intravaginal tablets, for induction of at-term labour. The Committee was informed that induction of labour is sometimes needed because of safety concerns for the mother or child. Methods of preparing the uterine cervix and inducing labour include: administration of oxytocin, prostaglandins, prostaglandin analogues, mifepristone, extra-amniotic saline solution infusion or mechanical procedures. When the condition of the cervix is unfavourable in the third trimester or when uterine evacuation is needed in the ﬁrst or second trimesters, oxytocin has a high failure rate for labour induction. In those cases, prostaglandin preparations have proved beneﬁ- cial, but most of them are expensive and unstable at room temperature. Misoprostol, dinoprostone and carboprost are used in the induction and augmentation of labour. The Committee noted that current evidence indicates that misoprostol is effective in cervical ripening and labour induction (52, 53). In an initial dose of 25 micrograms every four or six hours, vaginal misoprostol is more effective than oral and sublingual misoprostol. On the other hand, intravaginal misoprostol increases uterine hyperstimula- tion with or without changes in fetal heart rate. There are anecdotal reports of uterine rupture following treatment with prostaglandin analogues in women with or without previous caesarean section, but this is a very rare outcome. The Committee also noted that vaginal administration of misoprostol seems to be cost-effective, mainly because it reduces the incidence of operative deliveries which could lead

37 to further cost savings. The Committee recommended that misoprostol be administered as low-dose vaginal tablets, and be used only in organized health services with facilities to manage negative outcomes. The Committee stressed that vaginal use of the 200-microgram oral tablet for the same purpose is dangerous and should be discouraged. In view of the evidence of its efﬁcacy and safety, the Committee recommended that misoprostol vaginal tablet (25-microgram intravaginal tablet) be included on the complementary list of the Model List for the induction of at-term labour.

4.2.17 Nifedipine An application was received from the UNDP/UNFPA/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction, the WHO Department of Repro- ductive Health and Research and BMJ Knowledge for the inclusion of nifedipine tablet and capsule 10mg and 20mg, as a tocolytic on the Model List. Comments were received from Médecins Sans Frontières. The Committee noted that there is strong evidence to support the use of nifedipine to inhibit preterm labour. Nifedipine was studied in 10 randomized controlled trials in a Cochrane review (54). The results indicated that, compared with any other tocolytic agent (mainly betamimetics), nifedipine or nicardipine reduced the frequency of neonatal respiratory distress syndrome, necrotizing enterocolitis, intraventricular haemorrhage and neonatal jaundice. The Committee concluded that nifedipine is effective and safe for this indication, and noted that the sublingual route is pharmacologically equivalent to the conventional oral route (54) because the medicine is absorbed low in the gastrointestinal tract. The Committee recommended that nifedipine (10-mg immediate release capsules) be included on the Model List in the subsection of tocolytics.

4.2.18 Tenofovir Tenofovir had been proposed for addition to the Model List of antiretrovirals by the company developing the medicine. The applicant submitted additional information that the US Department of Health and Human Services had updated their guidelines for the use of antiretroviral agents to recommend the use of tenofovir as part of the nucleoside reverse transcriptase inhibitor (NRTI) backbone for both NRTI- and protease inhibitor (PI)-based regimens. Tenofovir was approved by the US Food and Drug Administration on 26 October 2001 and in Europe on 5 February 2002. A full application has been submitted. A report was submitted by the WHO Advisory Committee

38 on Safety of Medicines. The Committee also reviewed public statements by the European Agency for the Evaluation of Medicinal Products (EMEA) made on 30 July 2003 and 22 October 2003. The Committee noted that the data provided in the application were generally the sponsor’s summaries of the unpublished study reports that had been used as the basis of the regulatory review in the USA. References were not provided with the application and most of those cited were posters. An independent literature search carried out for this review identified several reports published over the last year that appear to include relevant information not provided in the application. These included case reports in relation to renal toxicity, a systematic review of the use of tenofovir in children and at least two observational studies of adverse effects and interactions. The safety data submitted in the application appeared to be based on a limited number of patients participating in the efficacy trials. The WHO Advisory Committee on Safety of Medicinal Products expressed concern about the acceptability and tolerability of adverse effects related to renal toxicity, interactions, lactic acidosis, bone problems and liver problems. In addition the EMEA had issued two public statements about tenofovir, concerning high rates of virologic failure with combinations of tenofovir and didanosine or lamivudine (55). On the basis of evidence available to the Agency at that time they advised against initiating new patients on a regimen containing tenofovir with didanosine or lamivudine. The Committee noted that tenofovir is mentioned in the WHO Guidelines on Scaling-up antiretroviral therapy in resource-limited settings: treatment guidelines for a public health approach 2003 revision, and that possible adverse effects and virologic failures are recognized. The guidelines state: As experience, availability and cost issues in resource-limited settings become clarified the inclusion of tenofovir (TDF) in WHO-recommended first-line regimens should be reconsidered. The Committee noted a lack of publicly available data to allow for an independent assessment of comparative effectiveness and safety. In particular there appear to be no published studies in highly relevant populations likely to use the product. As more complete data are likely to become available in the near future the Committee decided to defer its final recommendation to the next meeting in 2007.

4.2.19 Zinc sulfate An application was submitted by the WHO Department of Child and Adolescent Health and Development and UNICEF to include zinc

39 sulfate (tablets 10mg, 20mg) on the Model List for supplementation of treatment of childhood diarrhoea with oral rehydration salts (ORS). The Committee noted that there is adequate evidence to support the efﬁcacy of zinc sulfate supplementation as an adjunctive therapy in the treatment of acute and persistent non-dysenteric diarrhoea in children (56). Pooled analyses of trials showed that in children with acute diarrhoea who received zinc supplementation, the probability of continuing an episode of diarrhoea was 15% lower, and the probablility of persistent symptoms of chronic diarrhoea was 24% lower than in children who received no zinc supplementation. The Committee recommended that zinc sulfate (tablet or syrup in 10mg per unit dosage) be included on the Model List in the section on antidiarrhoeal drugs as a new subsection, with a footnote that in the treatment of children with acute diarrhoea, the product should only be used as an adjunct to ORS.

4.3 Other changes 4.3.1 Alcuronium and vecuronium The Committee noted that no systematic review is available to validate the comparative efﬁcacy and safety of alcuronium and vecuronium. The ISDB reviewer indicated that vecuronium offers advantages over alcuronium (57), and is therefore a better representative of neuromuscular blocking agents than alcuronium. However, the Committee noted that vecuronium is relatively expensive compared with the other alternatives. In view of the above considerations the Expert Committee recommended that alcuronium and vecuronium be retained with a square box on the Model List, and that a footnote should be added to alcuronium stating that alternative medicines for its possible replacement will be reviewed at its next meeting in 2007.

4.3.2 Antiretroviral medicines The Committee received a proposal from Médecins Sans Frontières to include speciﬁc pharmaceutical preparations better adapted to the situations in developing countries, such as non-refrigerated formulations, other improved dosage forms such as enteric-coated tablets; and once-a-day, time-released antiretroviral formulations in the antiretroviral section. The Committee recommended that the description in the Model List 2003 be revised as follows: In order to simplify treatment, facilitate storage and distribution, and improve patients’ adherence to the treatment plan, the Committee

40 recommends and endorses the use of fixed-dose combinations and the development of appropriate new fixed-dose combinations, including modified dosage forms, non-refrigerated formulations and paediatric formulations with assured pharmaceutical quality and interchangeability with single products as approved by the relevant medicine regulatory authority.

4.3.3 Ceftriaxone 1g injection An application was received from the WHO Department of Com- municable Disease Surveillance and Response, to add a dosage strength of 1g ceftriaxone for the treatment of epidemic meningococcal meningitis. The Committee noted that ceftriaxone 1g injection is at least thera- peutically equivalent to oily chloramphenicol for the immediate treatment of cases of meningococcal infection during an epidemic period and also in the treatment of children aged more than 2 months. However, the Committee also noted that widespread availability of low-cost ceftriaxone could lead to rapid emergence of resistance, given that this medicine can be used for several other indications. The Committee recommended that the dosage form of 1g ceftriaxone injection be included with the existing 250-mg injection on the complementary list.

4.3.4 Immunoglobulin, human normal During the Expert Committee Meeting in 2003, the Committee noted that there was no need for immunoglobulin in view of the availability of suitable vaccines, that there are no WHO clinical guidelines recommending its use, and that quality control of this blood product poses a problem. This assessment was based on the fact that immunoglobulin had been used in protection against hepatitis A, measles and, to a lesser extent, rubella. The Committee recommended that this item be deleted from the Model List. Applications for reinstatement were received, as immunoglobulin is used in the replacement and treatment of primary and secondary immunodeﬁciency syndromes. Full applications were received from the Plasma Protein Therapeutic Association (PPTA), the European Plasma Fractionation Association (EPFA) and the Immune Deﬁ- ciency Foundation (IDF), with the WHO Department of Blood Transfusion Safety as the focal point. Brief applications for reinstatement were received from many international unions and societies. A list of organizations supporting the reinstatement was submitted, consisting of groups from Canada, France, Ireland, Italy, the Netherlands, New Zealand and Spain.

41 The Committee noted Cochrane reviews which indicated that the efficacy of intravenous immunoglobulin was equal to that of plasma exchange for the treatment of Guillain-Barré syndrome (58), and the efficacy was equal to that of plasma exchange and prednisolone in the treatment of chronic inflammatory demyelinating polyradiculoneuropathy (59). A study involving 46 subjects who received 12 months of treatment for primary immunodeficiency showed that the use of immunoglobulin resulted in an estimated serious infection rate of 0.1 per subject per year (60). No data were submitted on the incidence rate of immunodeficiency diseases, but it was mentioned that the estimated prevalence rate in the USA of the total conditions needing immunoglobulin as replacement therapy and immunomodulation was approximately 3658 per million people (3.6/10000). No data were available from other parts of the world. The Committee noted that immunoglobulin is needed in the treatment of primary immunodeficiency, and is an alternative treatment to plasma exchange for secondary immunodeficiency. However, the Committee also noted that the individual and total prevalence of these diseases is very rare, that there is insufficient evidence of the efficacy of immunoglobulin despite its reported use, and that the cost of treatment is very high. On the basis of the above considerations, the Committee recommended that human immunoglobulin not be reinstated on the Model List.

4.3.5 Labetalol The starting point for this discussion was the discrepancy in the choice of beta-blockers between the 13th Model List and WHO clinical guidelines for the treatment of hypertension in pregnancy. A review was received from the Department of Reproductive Health and Research. The Committee noted that insufficient information was available on the efficacy of labetalol in the treatment of chronic hypertension in pregnancy (61). In the treatment of mild to moderate hypertension in pregnancy no significant difference in efficacy was found between the various antihypertensive medicines (62). Beta- blockers seem to be well tolerated by pregnant women. The Committee recommended no action at this stage, in view of the lack of evidence of better efficacy and safety of labetalol in the treatment of hypertension in pregnancy. The Committee also recommended that a full review of all medicines for the treatment of hypertension in pregnancy be discussed at the next meeting in 2007.

42 4.3.6 Prostaglandins for postpartum haemorrhage A statement on the status of prostaglandins for postpartum haemorrhage was received from the WHO Department of Reproductive Health and Research. The Committee noted that none of the prostaglandin analogues have been evaluated rigorously to identify benefits and harms when used in the treatment of postpartum haemorrhage. A Cochrane review (63) of 24 trials of misoprostol and eight of prostaglandin involving a total of 34203 participants indicated that neither intramuscular prostaglandins nor misoprostol is preferable to conventional injectable uterotonics as part of the active management of the third stage of labour, especially for low-risk women. A trial on the efficacy of prostaglandins in treatment of primary postpartum haemorrhage (64) showed that rectal misoprostol at a dose of 800 micrograms could be a useful first-line medicine. However, further randomized controlled trials are required to identify the best combinations of medicines, route of administration and dose for the treatment of postpartum haemorrhage. The Committee welcomed the fact that research is being undertaken on oral medicines to treat postpartum haemorrhage, and expressed its interest in reviewing future applications pertaining to medicines for treating this condition. In view of the lack of evidence presented in the current application, the Committee recommended that prostaglandins (i.e. misoprostol) for the treatment of postpartum haemorrhage should not be included in the Model List at this time.

5. Reviews of sections of the Model List

5.1 Beta-lactam medicines During its meeting in 2003, the Committee noted that there was a need to review the cefalosporins on the Model List. An extensive review was undertaken by the ISDB. The review proposed that ceftazidime and ceftriaxone be retained on the Model List, and also that cefalexin and cefazolin be included on the Model List. Cefalexin was proposed as an alternative to amoxicillin/ampicillin and cefazolin as an alternative for surgical prophylaxis. Following the procedures of the Expert Committee prior to 2002, cefazolin and cefalexin would probably have been added to the 14th Model List based on the information in this section review and the opinion of the Committee. In keeping with the importance of its procedures, which require that full information be included in an

43 application for addition, and recognizing the resulting lack of balance in the list with the current inclusion of ceﬁxime (see section 4.2.2), the Committee accepted the recommendation of the reviewer and requested that a formal application for these two medicines be submitted for the next meeting, and that a footnote to this effect be added to the Model List.

5.2 General anaesthetics and oxygen During its meeting in 2003, the Expert Committee noted that there was a need to review the anaesthetics section of the Model List. A review was undertaken by the ISDB. Based on the review, the Com- mittee recommended that ether be deleted (see section 4.1.11) while all other medicines in this section be retained on the Model List. A short-acting intravenous agent, propofol, is now cheaper than sodium thiopentone and is included on the essential medicines lists of many countries. The Expert Committee recommended that an application for propofol be submitted for its meeting in 2007.

5.3 Muscle relaxants During its meeting in 2003, the Committee noted that there was a need to review the muscle relaxants section. Based on a detailed review by the ISDB, the Committee recommended that suxamethonium chloride and neostigmine metilsulfate be retained on the Model List, and requested that applications for atracurium and pancuronium, which could possibly replace alcuronium, be submitted to its meeting in 2007 (see below). In this application due regard should be given to the relative lack of heat stability of atracurium and to comparative cost information.

5.4 Ophthalmological preparations During its meeting in 2003, the Committee noted that there was a need to review the ophthalmology section. Unfortunately the review had not been completed and was therefore not discussed. The Com- mittee requested that this section be reviewed at the next meeting.

6. Rare diseases The Committee considered the issue of rare diseases as a result of concerns expressed about the possible deletion of factor VIII and factor IX and medicines for other rare diseases also known as “orphan diseases”. The Committee reviewed the discussion paper entitled Rare essentials? Drugs for rare diseases on the Essential

44 Medicines List (65). The Committee made a distinction between “neglected diseases” which may not be rare in some geographical areas1 and rare diseases which have a prevalence of fewer than 5 per 10000 worldwide. Medicines for neglected diseases may be considered as essential medicines. The Committee acknowledged that the recognition of rare diseases may increase in importance as diagnostics improve, access to health systems increases and communicable diseases decline in importance. Countries are likely to seek advice from WHO as to how to address this issue. The Committee suggested that there was a need for WHO to establish a policy advisory group on rare diseases to study this issue.

7. Future priorities The Committee recommended that full applications for addition of the following items be submitted to the Committee for consideration at its next meeting in 2007: (1) propofol, (6.2.1) cefalexin, cefazolin;

(6.4.2) emtricitabine, tenofovir and combination; (7.1) 5 HT1 agonist (triptan(s)); (12.2) amiodarone, sotalol; (20) atracurium, pancuronium; (27) oral calcium. The Committee recommended that the following section reviews be prepared and submitted for discussion at its next meeting in 2007: Section 4: antidotes; Section 6.4: medicines for MDR-TB; Section 11.1: colloids versus crystalloids; Section 12.2: anti-arrhythmic medicines; Section 12.3: medicines for hypertension in pregnancy, and also the continued use of the square box for amlodipine; Section 12.4: medicines used for cardiac failure; Section 17.7.2: antidiarrhoeals in adults; Section 18.3: contraceptives; Section 21: ophthalmological preparations.

7.1 Summary of recommendations — additions, changes and deletions to the Model List 1. The Committee recommended that the following medicines be deleted from the Model List: (1.1) ether

1 This deﬁnition is derived from orphan drug legislation in the European Union and the USA.

45 (2.3) colchicine (5) clonazepam (6.2.2) nalidixic acid (6.2.5) thioacetazone + isoniazid (6.6) diethyltoluamide (7.1) ergotamine (11.1) polygeline (12.2) isoprenaline (13.7) sun protection agents (17.3) local anaesthetics, astringent, anti-inﬂammatory as antihaemorrhoidal (17.4) atropine as spasmolytic (21.1) silver nitrate eye solution (22.1) ergometrine tablet (22.2.2) salbutamol as tocolytic (25) theophylline, aminophylline, cromoglicic acid.

2. The Committee recommended that the following changes be made in items already on the Model List: (6.1.1) niclosamide: remove footnote on future review (6.1.1) pyrantel: remove footnote on future review (6.1.3) oxamniquine: remove footnote on future review; triclabendazole: remove footnote on future review (6.2.1) ceftriaxone: add 1g injection (6.2.1) imipenem + cilastatin: remove footnote on future review (6.2.2) spectinomycin: remove footnote on future review (6.2.4) levoﬂoxacin: remove footnote on future review (11.1) dextran 70: add square box (11.2) factors VIII and IX concentrates: remove footnote on future review (12.2) antiarrhythmic medicines: add footnote that section will be reviewed at next meeting (12.3) nifedipine: replace with amlodipine with square box (12.4) heart failure: add furosemide (tablet and injection, as under diuretics) (17.7) change section name to: “Antidiarrhoeal (symptomatic) medicines for adults” (18.3.1) subsection “hormonal” to be divided into two subsections: oral, injectable medroxyprogesterone acetate (depot injection): move to core list, remove footnote on future review; (18.4) ethinyloestradiol: add footnote on future review (18.7) norethisterone: add footnote on future review; medroxyprogesterone acetate: add footnote on future review

46 (20) alcuronium: add footnote that potential alternatives will be reviewed in 2007 (27) sodium fluoride: change description to “in any appropriate topical formulation”; remove square box and remove footnote on future review, calcium gluconate: remove footnote on future review. 3. The Committee recommended that the following medicines be added to the 14th Model List: (6.2.1) cefixime tablet 400mg (6.3) clotrimazole 1%, 10% vaginal cream; 100mg, 500mg vaginal tablets (17.5.2) zinc sulfate tablet or syrup in 10mg per unit dosage (22.1) misoprostol 25 microgram intravaginal tablet on complementary list; mifepristone 200mg oral tablet — misoprostol 200 microgram vaginal tablet on the complementary list with the footnote “Requires close medical supervision”: in reviewing the recommendation relating to this combination of products, the Director-General decided to add a note adjacent to the combination in the WHO Model List stating “Where permitted under national law and where culturally acceptable”. (22.2) nifedipine 10mg capsule as tocolytic (24.5) methadone oral solution 5mg/5ml, 10mg/5ml, or concentrate for oral solution 5mg/ml, 10mg/ml on complementary list, with square box to cover buprenorphine, within a new subsection “Medicines used in substance dependence programmes” and a footnote that these products should be used only within an established support programme. 4. The Committee decided to defer its recommendations on the following items, and requested that more information be submitted at its next meeting in 2007: (6.4.2) tenofovir, emtricitabine, tenofovir + emtrictabine (25) caffeine citrate. 5. The Committee recommended that the following applications be rejected: (2.1) ibuprofen paediatric suspension (2.1) methoxyflurane (6.5.2) miltefosine (12.3) labetalol (18.3.1) combination injectable contraceptives, etonogestrel- releasing implant, levonorgestrel-releasing implant, levonorgestrel-releasing IUD (19.2) immunoglobulin, human normal.

47 6. The Committee recommended that full applications for addition of the following items be submitted to the Committee for consideration at its next meeting in 2007: (1) propofol, (6.2.1) cefalexin, + cefazolin; (6.4.2) emtricitabine tenofovir; (7.1) 5 HT1 agonist (triptan(s)); (12.2) amiodarone, sotalol; (20) atracurium, pancuronium; (27) oral calcium. 7. The Committee recommended that the following section reviews be prepared and submitted for discussion at its next meeting in 2007: Section 4: antidotes Section 6.2.4: medicines for MDR-TB Section 11.1: colloids versus crystalloids Section 12.2: anti-arrhythmic medicines Section 12.3: medicines for hypertension in pregnancy and also the continued use of the square box for amlodipine Section 12.4: medicines used for cardiac failure Section 17.7.2: antidiarrhoeals in adults Section 18.3: contraceptives Section 21: ophthalmological preparations.

7.2 Methodological issues 1. The Committee recommended that section reviews should, as far as possible, be performed in the ﬁrst year after a Committee meeting, so that full applications for new additions, if suggested by the section review, can be prepared in time for submission to the Committee meeting at the same time as the section review. 2. The Committee recommended that a policy advisory group on rare disease be established to study the issue of effective medicines for life-threatening rare diseases. 3. The Committee recommended that the original applications and other supporting documents for the Expert Committee published on the WHO web site be maintained on the web site for readers of the report who wish to see these materials, and that a permanent record be created as well.

7.3 Rational medicine use The Committee recommended that WHO encourages and supports Member States in developing and implementing effective strategies and national programmes to improve access to and use of quality medicines, and that WHO urgently identify potential sources of funding and donor support to develop a workplan for this key area.

48 References

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53 © World Health Organization WHO Technical Report Series, No. 933, 2006

Annex 1 The 14th WHO Model List of Essential Medicines

Introduction The concept of essential medicines Essential medicines are those that satisfy the priority health care needs of the population. They are selected with due regard to public health relevance, evidence on efﬁcacy and safety, and comparative cost-effectiveness. Essential medicines are intended to be available within the context of functioning health systems at all times in adequate amounts, in the appropriate dosage forms, with assured quality and adequate information, and at a price the individual and the community can afford. The implementation of the concept of essential medicines is intended to be ﬂexible and adaptable to many different situations; exactly which medicines are regarded as essential remains a national responsibility. Experience has shown that careful selection of a limited range of essential medicines results in a higher quality of care, better management of medicines (including improved quality of prescribed medicines), and a more cost-effective use of available health resources.

The WHO Model List of Essential Medicines Most countries require that a pharmaceutical product be approved on the basis of efﬁcacy, safety and quality before it can be prescribed. The majority of health care and insurance schemes will only cover the cost of medicines on a given list of approved medicines. Medicines on such lists are selected after careful study of the medicines used to treat particular conditions and a comparison of the value they provide in relation to their cost. The WHO Model List of Essential Medicines (the Model List) is an example of such a list. The ﬁrst WHO Model List was drawn up in 1977 in response to a request from the World Health Assembly (resolution WHA28.66) to the Director-General of WHO to provide Member States with advice on the selection and procurement, at reasonable costs, of essential medicines of established quality corresponding to their national health needs. The Model List has since been revised and updated at intervals of approximately two years. Over the past two decades, the

54 regular updating of the Model List has not only been at the heart of WHO’s revised drug strategy but has also formed a key component of the information required by Member States in relation to their medicine procurement and supply programmes. The Model List was originally intended as a guide for the development of national and institutional essential medicine lists. It was not designed as a global standard. Nevertheless, since its introduction the Model List has led to a global acceptance of the concept of essential medicines as a powerful tool for promoting health equity. By the end of 2003, 156 Member States had official essential medicines lists, of which 99 had been updated in the previous five years. Most countries have national lists; some have provincial or state lists as well. The concept of essential medicines has also been adopted by many international organizations, including the United Nations Children’s Fund (UNICEF) and the Office of the United Nations High Commis- sioner for Refugees (UNHCR), as well as by nongovernmental organizations and international non-profit supply agencies. Many of these organizations base their medicine supply system on the Model List. Lists of essential medicines also guide the procurement and supply of medicines in the public sector, schemes that reimburse medicine costs, medicine donations and local medicine production, and, furthermore, are widely used as informational and educational tools by health professionals. Health insurance schemes too are increasingly using national lists of essential medicines for reference purposes. The way in which national lists of essential medicines are developed and used has evolved over time. Initially, lists were drawn up primarily as a means to guide the procurement of medicines. More recently, however, greater emphasis has been placed on the development of treatment guidelines as the basis for medicine selection and supply, and on the evidence underlying the development of those treatment guidelines. Consequently, there has been an increasing demand for information on why a particular medicine is included in the Model List and also for references to the underlying evidence. Activities are now underway to strengthen the links between the Model List and the treatment guidelines developed by WHO. In its present form, the Model List aims to identify cost-effective medicines for priority conditions, together with the reasons for their inclusion, linked to evidence-based clinical guidelines and with special emphasis on public health aspects and considerations of value for money. Information that supports the selection of essential medicines, such as relevant WHO clinical guidelines, systematic reviews, key references and indicative cost information is being made

55 available via the WHO web site as the WHO Essential Medicines Library. The latter provides links to other relevant sources of information, including the WHO model formulary and information on nomenclature and quality assurance standards. The Essential Medi- cines Library is under construction and will be expanded over time. Its primary function is to facilitate the work of national and institutional committees in developing national and institutional lists of essential medicines. Medicines on the Model List are classified as either “core” list or “complementary” list medicines. The core list presents a list of minimum medicine needs for a basic health care system, listing the most efficacious, safe and cost-effective medicines for priority conditions. Priority conditions are selected on the basis of current and estimated future public health relevance, and potential for safe and cost- effective treatment. The complementary list presents essential medicines for priority diseases, for which specialized diagnostic or monitoring facilities and/or specialist medical care and/or specialist training are needed. In case of doubt, medicines may also be listed as complementary on the basis of consistently higher costs or less attractive cost-effectiveness in a variety of settings. A number of medicines are labelled with a square box symbol. This symbol is primarily intended to indicate similar clinical performance within a pharmacological class. The listed medicine should be the example of the class for which there is the best evidence for effectiveness and safety. In some cases, this may be the first medicine that is licensed for marketing; in others, subsequently licensed compounds may be safer or more effective. Where there is no difference in terms of the efficacy and safety data, the listed medicine should be the one that is generally available at the lowest price, based on international drug price information sources. Therapeutic equivalence is only indicated on the basis of reviews of efficacy and safety and when consistent with WHO clinical guidelines. National lists should not use a similar symbol and should be specific in their final selection, which would depend on local availability and price. Examples of alternatives for the medicines with a square box symbol are not included in the Model List, but such information is provided in the WHO model formulary and in the Essential Medicines Library.

Procedures for updating the Model List The procedures for updating the Model List are in line with the WHO recommended process for developing clinical practice guidelines. The key components are a systematic approach to collecting and review-

56 ing evidence and a transparent development process with several rounds of external review. The procedures are intended to serve as a model for developing or updating national and institutional clinical guidelines and lists of essential medicines. Further information on the procedures for updating the Model List, including descriptions of the applications and details of the review process, is available from the WHO web site.

Selection criteria The choice of essential medicines depends on several factors, including public health relevance and the availability of data on the efficacy, safety and comparative cost-effectiveness of available treatments. Factors such as stability in various conditions, the need for special diagnostic or treatment facilities and pharmacokinetic proper- ties are also considered if appropriate. In adapting the Model List to their own needs, countries often consider factors such as local demog- raphy and the pattern of prevalent diseases; treatment facilities; training and experience of available personnel; local availability of individual pharmaceutical products; financial resources; and environ- mental factors. The selection of essential medicines must be based on valid scientific evidence; only medicines for which sound and adequate data on efficacy and safety are available should be selected. In the absence of adequate scientific evidence on current treatment of a priority disease, the WHO Expert Committee on the Selection and Use of Essen- tial Medicines may either defer its decision regarding selection until more evidence becomes available, or choose to make recommendations based on expert opinion and experience. Most essential medicines should be formulated as single compounds. Fixed-dose combination products are selected only when the combination has a proven advantage over single compounds administered separately in therapeutic effect, safety, adherence or in delaying the development of drug resistance in malaria, tuberculosis and HIV/ AIDS. When making cost comparisons between medicines, the cost of the total treatment, not just the unit cost of the medicine, is considered. Cost and cost-effectiveness comparisons may be made among alternative treatments within the same therapeutic group, but are generally not made across therapeutic categories (e.g. between the treatment of tuberculosis and the treatment of malaria). The absolute cost of the treatment does not constitute a reason to exclude a medicine from the Model List that otherwise meets the stated selected criteria. The

57 patent status of a medicine is not considered when selecting medicines for the Model List.

Quality assurance Priority should be given to ensuring that available medicines have been made according to good manufacturing practices and are of assured quality. Factors that need to be considered include: — knowledge of, and conﬁdence in, the origin of the product; — the pharmaceutical stability of the product, particularly in the environment that it will be used; — where relevant, bioavailability and bioequivalence information. It is recommended that all medicines be purchased from known manufacturers, their duly accredited agents, or recognized international agencies known to apply high standards in selecting their suppliers.

Promoting rational use of essential medicines The selection of essential medicines is only one step towards the improvement of the quality of health care; selection needs to be followed by appropriate use. Each individual should receive the right medicine, in an adequate dose for an adequate duration, with appropriate information and follow-up treatment, and at an affordable cost. Within different countries and settings, this is inﬂuenced by a number of factors, such as regulatory decisions, procurement, information, training, and the context in which medicines are prescribed or recommended.

Training, education and the provision of medicines information To ensure the safe, effective and prudent use of essential medicines, access to relevant, reliable and independent information on medicines is vital. Health care professionals should receive education about the use of medicines not only during their training but also throughout their careers. The more highly trained individuals should be encouraged to assume responsibility for educating those with less training. Health care providers and pharmacists who are responsible for dispensing medicines should take every opportunity to inform consumers about the rational use of products, including those for self- medication, at the time they are dispensed. Governments, universities and professional associations have a critical role to play with regard to the improvement of undergraduate, postgraduate and continuing education in clinical pharmacology,

58 therapeutics and medicines information issues. Problem-based pharmacotherapy teaching has been shown to be a particularly effective strategy in this area. Well presented and appropriate information about medicines not only ensures that they are used properly but also decreases the inap- propriate use of medicines. Health ministries have a responsibility to arrange for the provision of such information. Independent medicines information activities should also be properly funded and, if necessary, ﬁnanced through health care budgets. Electronic, readily accessible sources of medicines information are becoming more widely available and can form the basis of reliable medicines information systems in many settings.

Standard clinical guidelines Standard clinical guidelines are an effective tool for assisting health professionals to choose the most appropriate medicine for a given patient with a given condition. They should be developed at national and local levels and updated on a regular basis. In order to be effective, however, standard clinical guidelines require the support of appropriate education and training programmes aimed at encouraging their use.

Drug and therapeutics committees Drug and therapeutics committees can play an important role in the development and implementation of effective essential medicines programmes. Such committees should be encouraged to select products for local use from a national essential medicines list, to measure and monitor the use of these products in their own environments and to undertake interventions to improve their rational use. There is good evidence to suggest that involving both drug and therapeutics committees and prescribers in guideline development can contribute to improved prescribing behaviour.

Measuring and monitoring medicine use The purpose of drug utilization studies is to examine the development, regulation, marketing, distribution, prescription, dispensing and use of medicines within a society, with special emphasis on the medical, social and economic consequences. Studies of this type consider all levels of the therapeutic chain, from the development of medicines to their use by consumers. Drug utilization studies can be medicine-oriented (i.e. focused on the use of a particular medicine or group of medicines) or problem-oriented (i.e. focused on the treatment of a particular condition or disease)

59 and can provide consumption indicators for a given country, area or institution. Consumption can be measured in terms of economic expenditure (either in absolute terms or as a percentage of the total health bud- get), the number of units, or as Defined Daily Doses (DDDs). How- ever, it is generally recommended that drug utilization studies be conducted using the Anatomical Therapeutic Chemical (ATC) classification and the DDD as the measuring unit, especially when making international comparisons on the use of medicines. The efficacy of a medicine is best assessed on the basis of randomized clinical trials, which, if well conducted, provide reliable estimates of the treatment effect of a new medicine. However, clinical trials cannot be conducted in all possible populations or settings and therefore their results must be translated into routine clinical practice with care. Given that drug utilization studies generally provide evidence on the use and the effects of medicines in routine conditions, they can provide additional evidence for the evaluation of the effectiveness of a medicine. Drug utilization studies and clinical trials are important tools for identifying those factors or elements of the therapeutic chain in need of improvement or change. The results of such studies should be taken into consideration when taking regulatory action, selecting medicines, or designing information, training and teaching programmes.

Monitoring of medicine safety and pharmacovigilance Safety monitoring is an important part of the overall surveillance of medicine use. The aims of the various forms of pharmacovigilance are to identify new, previously unrecognized adverse effects of medicines, to quantify their risks, and to communicate these to drug regulatory authorities, health professionals, and, when relevant, the public. Vol- untary reporting of adverse effects of medicines, on which the Inter- national WHO Programme for Drug Monitoring is based, has been effective in identifying a number of previously undescribed effects. Voluntary reporting schemes, together with other methods for assem- bling case series, can identify certain local safety problems, and thus form the basis for speciﬁc regulatory or educational interventions. The magnitude of the risk of adverse effects is generally evaluated using observational epidemiological methods, such as case–control, cohort and case–population studies. Each country and institution should set up simple schemes aimed at identifying problems related to the safety of medicines.

60 Explanatory notes The core list presents a list of minimum medicine needs for a basic health care system, listing the most efficacious, safe and cost-effective medicines for priority conditions. Priority conditions are selected on the basis of current and estimated future public health relevance, and potential for safe and cost-effective treatment. The complementary list presents essential medicines for priority diseases, for which specialized diagnostic or monitoring facilities, and/or specialist medical care, and/or specialist training are needed. In case of doubt medicines may also be listed as complementary on the basis of consistently higher costs or less attractive cost-effectiveness in a variety of settings. When the strength of a medicine is specified in terms of a selected salt or ester, this is mentioned in brackets; when it refers to the active moiety, the name of the salt or ester in brackets is preceded by the word “as”. The square box symbol () is primarily intended to indicate similar clinical performance within a pharmacological class. The listed medicine should be the example of the class for which there is the best evidence for effectiveness and safety. In some cases, this may be the first medicine that is licensed for marketing; in other instances, subsequently licensed compounds may be safer or more effective. Where there is no difference in terms of efficacy and safety data, the listed medicine should be the one that is generally available at the lowest price, based on international drug price information sources. Thera- peutic equivalence is only indicated on the basis of reviews of efficacy and safety and when consistent with WHO clinical guidelines. Na- tional lists should not use a similar symbol and should be specific in their final selection, which would depend on local availability and price. Medicines are listed in alphabetical order, within sections.

61 1. Anaesthetics 1.1 General anaesthetics and oxygen halothane inhalation ketamine injection, 50 mg (as hydrochloride)/ml in 10-ml vial nitrous oxide inhalation oxygen inhalation (medicinal gas) thiopental powder for injection, 0.5 g, 1.0 g (sodium salt) in ampoule 1.2 Local anaesthetics bupivacaine injection, 0.25%, 0.5% (hydrochloride) in vial injection for spinal anaesthesia, 0.5% (hydrochloride) in 4-ml ampoule to be mixed with 7.5% glucose solution lidocaine injection, 1%, 2% (hydrochloride) in vial injection for spinal anaesthesia, 5% (hydrochloride) in 2-ml ampoule to be mixed with 7.5% glucose solution topical forms, 2–4% (hydrochloride) lidocaine + epinephrine injection 1%, 2% (hydrochloride) + (adrenaline) epinephrine 1 : 200 000 in vial dental cartridge 2% (hydrochloride) + epinephrine 1 : 80 000 Complementary list ephedrine injection, 30 mg (hydrochloride)/ml in 1-ml ampoule (for use in spinal anaesthesia during delivery, to prevent hypotension) 1.3 Preoperative medication and sedation for short-term procedures atropine injection, 1 mg (sulfate) in 1-ml ampoule diazepam injection, 5 mg/ml in 2-ml ampoule tablet, 5 mg morphine injection, 10 mg (sulfate or hydrochloride) in 1-ml ampoule promethazine elixir or syrup, 5 mg (hydrochloride)/5 ml

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

62 2. Analgesics, antipyretics, non-steroidal anti-inﬂammatory medicines, medicines used to treat gout and disease modifying agents used in rheumatoid disorders 2.1 Non-opioids and non-steroidal anti-inﬂammatory medicines acetylsalicylic acid tablet, 100–500 mg suppository, 50–150 mg ibuprofen tablet, 200 mg, 400 mg paracetamola tablet, 100–500 mg suppository, 100 mg syrup, 125 mg/5 ml 2.2 Opioid analgesics codeine tablet, 30 mg (phosphate) morphine injection, 10 mg (sulfate or hydrochloride) in 1-ml ampoule oral solution, 10 mg (hydrochloride or sulfate)/5 ml tablet, 10 mg (sulfate) 2.3 Medicines used to treat gout allopurinol tablet, 100 mg 2.4 Disease-modifying agents used in rheumatoid disorders chloroquine tablet, 100 mg, 150 mg (as phosphate or sulfate) Complementary list azathioprine tablet, 50 mg methotrexate tablet, 2.5 mg (as sodium salt) penicillamine capsule or tablet, 250 mg sulfasalazine tablet, 500 mg

3. Antiallergics and medicines used in anaphylaxis chlorphenamine tablet, 4 mg (hydrogen maleate) injection, 10 mg (hydrogen maleate) in 1-ml ampoule dexamethasone injection, 4 mg dexamethasone phosphate (as disodium salt) in 1-ml ampoule

a Not recommended for anti-inﬂammatory use due to lack of proven beneﬁt to that effect. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

63 3. Antiallergics and medicines used in anaphylaxis (continued) epinephrine (adrenaline) injection, 1 mg (as hydrochloride or hydrogen tartrate) in 1-ml ampoule hydrocortisone powder for injection, 100 mg (as sodium succinate) in vial prednisolonea tablet, 5 mg, 25 mg

4. Antidotes and other substances used in poisonings Section 4 will be reviewed at the next meeting of the Expert Committee. 4.1 Non-speciﬁc charcoal, activated powder 4.2 Speciﬁc acetylcysteine injection, 200 mg/ml in 10-ml ampoule atropine injection, 1 mg (sulfate) in 1-ml ampoule calcium gluconate injection, 100 mg/ml in 10-ml ampoule deferoxamine powder for injection, 500 mg (mesilate) in vial dimercaprol injection in oil, 50 mg/ml in 2-ml ampoule

DL-methionine tablet, 250 mg methylthioninium chloride injection, 10 mg/ml in 10-ml ampoule (methylene blue) naloxone injection, 400 micrograms (hydrochloride) in 1-ml ampoule penicillamine capsule or tablet, 250 mg potassium ferric hexacyano- powder for oral administration

ferrate(II)·2H20 (Prussian blue) sodium calcium edetate injection, 200 mg/ml in 5-ml ampoule sodium nitrite injection, 30 mg/ml in 10-ml ampoule sodium thiosulfate injection, 250 mg/ml in 50-ml ampoule

5. Anticonvulsants/antiepileptics carbamazepine scored tablet, 100 mg, 200 mg diazepam injection, 5 mg/ml in 2-ml ampoule (intravenous or rectal) magnesium sulfateb injection, 500 mg/ml in 2-ml ampoule, 500 mg/ml in 10-ml ampoule a There is no evidence for complete clinical similarity between prednisolone and dexamethasone at high doses. b For use in eclampsia and severe pre-eclampsia and not for other convulsant disorders. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

64 5. Anticonvulsants/antiepileptics (continued) phenobarbital tablet, 15–100 mg elixir, 15 mg/5 ml phenytoin capsule or tablet, 25 mg, 50 mg, 100 mg (sodium salt) injection, 50 mg/ml in 5-ml vial (sodium salt) valproic acid enteric coated tablet, 200 mg, 500 mg (sodium salt) Complementary list ethosuximide capsule, 250 mg syrup, 250 mg/5 ml

6. Anti-infective medicines 6.1 Anthelminthics 6.1.1 Intestinal anthelminthics albendazole chewable tablet, 400 mg levamisole tablet, 50 mg, 150 mg (as hydrochloride) mebendazole chewable tablet, 100 mg, 500 mg niclosamidea chewable tablet, 500 mg praziquantel tablet, 150 mg, 600 mg pyrantel chewable tablet, 250 mg (as embonate) oral suspension, 50 mg (as embonate)/ml

6.1.2 Antiﬁlarials ivermectin scored tablet, 3 mg, 6 mg Complementary list diethylcarbamazine tablet, 50 mg, 100 mg (dihydrogen citrate) suramin sodium powder for injection, 1 g in vial

6.1.3 Antischistosomals and other antitrematode medicine praziquantel tablet, 600 mg triclabendazole tablet, 250 mg

a Niclosamide is listed for use when praziquantel treatment fails. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

65 6. Anti-infective medicines (continued) Complementary list oxamniquinea capsule, 250 mg syrup, 250 mg/5 ml 6.2 Antibacterials 6.2.1 b-Lactam medicinesb amoxicillin capsule or tablet, 250 mg, 500 mg (anhydrous) powder for oral suspension, 125 mg (anhydrous)/5 ml amoxicillin + clavulanic acid tablet, 500 mg + 125 mg ampicillin powder for injection, 500 mg, 1 g (as sodium salt) in vial benzathine benzylpenicillin powder for injection, 1.44 g benzylpenicillin (= 2.4 million IU) in 5-ml vial benzylpenicillin powder for injection, 600 mg (= 1 million IU), 3 g (= 5 million IU) (sodium or potassium salt) in vial ceﬁximec capsule 400 mg cloxacillin capsule, 500 mg, 1 g (as sodium salt) powder for oral solution, 125 mg (as sodium salt)/5 ml powder for injection, 500 mg (as sodium salt) in vial phenoxymethylpenicillin tablet, 250 mg (as potassium salt) powder for oral suspension, 250 mg (as potassium salt)/5 ml procaine benzylpenicillin powder for injection, 1 g (= 1 million IU), 3g (= 3 million IU) in vial Complementary list ceftazidime powder for injection, 250 mg (as pentahydrate) in vial

a oxamniquine is listed for use when praziquantel treatment fails. b Applications for cefalexin and cefazolin are anticipated for the next meeting of the Expert Committee. c Only listed for single-dose treatment of uncomplicated ano-genital gonorrhoea. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

66 6. Anti-infective medicines (continued) ceftriaxone powder for injection, 250 mg, 1 g (as sodium salt) in vial imipenema + cilastatina powder for injection 250 mg (as monohydrate) + 250 mg (as sodium salt), 500 mg (as monohydrate) + 500 mg (as sodium salt) in vial 6.2.2 Other antibacterials azithromycinb capsule, 250 mg or 500 mg suspension 200 mg/5 ml chloramphenicol capsule, 250 mg oral suspension, 150 mg (as palmitate)/ 5ml powder for injection, 1 g (sodium succinate) in vial oily suspension for injection, 0.5 g (as sodium succinate)/ml in 2-ml ampoule ciproﬂoxacinc tablet 250 mg (as hydrochloride) doxycyclinec capsule or tablet, 100 mg (hydrochloride) erythromycin capsule or tablet, 250 mg (as stearate or ethyl succinate) powder for oral suspension, 125 mg (as stearate or ethyl succinate) powder for injection, 500 mg (as lactobionate) in vial gentamicinc injection, 10 mg, 40 mg (as sulfate)/ml in 2-ml vial metronidazole tablet, 200–500 mg injection, 500 mg in 100-ml vial suppository, 500 mg, 1 g oral suspension, 200 mg (as benzoate)/ 5ml nitrofurantoin tablet, 100 mg spectinomycin powder for injection, 2 g (as hydrochloride) in vial

a Only listed for the treatment of life-threatening hospital-based infection due to suspected or proven multidrug-resistant infection. b Only listed for single-dose treatment of genital Chlamydia trachomatis and of trachoma. c Final selection depends on indication for use. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

67 6. Anti-infective medicines (continued) sulfamethoxazole + trimethoprim tablet, 100 mg + 20 mg, 400 mg + 80 mg oral suspension, 200 mg + 40 mg/5 ml injection, 80 mg + 16 mg/ml in 5-ml and 10-ml ampoules trimethoprim tablet, 100 mg, 200 mg Complementary list clindamycin capsule, 150 mg injection, 150 mg (as phosphate)/ml sulfadiazine tablet, 500 mg injection, 250 mg (sodium salt) in 4-ml ampoule vancomycin powder for injection, 250 mg (as hydrochloride) in vial 6.2.3 Antileprosy medicines Medicines used in the treatment of leprosy should never be used except in combination. Combination therapy is essential to prevent the emergence of drug resistance. Colour-coded blister packs (multidrug therapy (MDT) blister packs) containing standard two-medicine (paucibacillary leprosy) or three-medicine (multibacillary leprosy) combinations for adult and childhood leprosy should be used. MDT blister packs can be supplied free of charge through WHO. clofazimine capsule, 50 mg, 100 mg dapsone tablet, 25 mg, 50 mg, 100 mg rifampicin capsule or tablet, 150 mg, 300 mg 6.2.4 Antituberculosis medicines ethambutol tablet, 100–400 mg (hydrochloride) isoniazid tablet, 100–300 mg isoniazid + ethambutol tablet, 150 mg + 400 mg pyrazinamide tablet, 400 mg rifampicin capsule or tablet, 150 mg, 300 mg rifampicin + isoniazid tablet, 60 mg + 30 mg; 150 mg + 75 mg; 300 mg + 150 mg; 60 mg + 60 mg;a 150 mg + 150 mga

a For intermittent use three times weekly. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

68 6. Anti-infective medicines (continued) rifampicin + isoniazid + pyrazinamide tablet, 60 mg + 30 mg + 150 mg; 150 mg + 75 mg + 400 mg 150 mg + 150 mg + 500 mga rifampicin + isoniazid + tablet, 150 mg + 75 mg + 400 mg pyrazinamide + ethambutol + 275 mg streptomycin powder for injection, 1 g (as sulfate) in vial Complementary list amikacinb powder for injection, 1000 mg in vial p-aminosalicylic acid b tablet, 500 mg; granules, 4 g in sachet capreomycinb powder for injection, 1000 mg in vial ciprofloxacinb tablet, 250 mg, 500 mg cycloserineb capsule or tablet, 250 mg ethionamideb tablet, 125 mg, 250 mg kanamycinb powder for injection, 1000 mg in vial levofloxacinb tablet, 250 mg, 500 mg ofloxacinb tablet, 200 mg, 400 mg 6.3 Antifungal medicines clotrimazole vaginal tablet, 100 mg, 500 mg vaginal cream, 1%, 10% fluconazole capsule, 50 mg injection, 2 mg/ml in vial oral suspension, 50 mg/5ml griseofulvin capsule or tablet, 125 mg, 250 mg nystatin tablet, 100 000IU, 500 000 IU lozenge 100 000 IU pessary, 100 000 IU Complementary list amphotericin B powder for injection, 50 mg in vial

a For intermittent use three times weekly. b Reserve second-line medicine for the treatment of multidrug-resistant tuberculosis (MDR-TB) should be used in specialized centres adhering to WHO standards for TB control. These medicines will be reviewed at the next meeting of the Expert Committee. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

69 6. Anti-infective medicines (continued) flucytosine capsule, 250 mg infusion, 2.5 g in 250 ml potassium iodide saturated solution 6.4 Antiviral medicines 6.4.1 Antiherpes medicines aciclovir tablet, 200 mg; powder for injection, 250 mg (as sodium salt) in vial 6.4.2 Antiretroviral medicines The antiretroviral medicines do not cure the HIV infection, they only temporarily suppress viral replication and improve symptoms. They have various adverse effects and patients receiving these medicines require careful monitoring by adequately trained health professionals. For these reasons, continued rigorous promotion of measures to prevent new infections is essential and the need for this has not been diminished in any way by the addition of antiretroviral medicines to the Model List. Adequate resources and trained health professionals are a prerequisite for the introduction of this class of medicines. Effective therapy requires commencement of three or four medicines simultaneously, and alternative regimens are necessary to meet specific requirements at start-up, to substitute for first-line regimens in the case of toxicity, or to replace failing regimens. In order to simplify treatment, facilitate storage and distribution, and improve patients’ adherence to the treatment plan, the Committee recommends and endorses the use of fixed-dose combinations and the development of appropriate new fixed-dose combinations. These include modified dosage forms, non-refrigerated formulations and paediatric formulations with assured pharmaceutical quality and interchangeability with the single products as approved by the relevant drug regulatory authority. 6.4.2.1 Nucleoside reverse transcriptase inhibitors abacavir (ABC) tablet, 300 mg (as sulfate) oral solution, 100 mg (as sulfate)/5 ml didanosine (ddI) buffered chewable, dispersible tablet, 25 mg, 50 mg, 100 mg, 150 mg, 200 mg buffered powder for oral solution, 100 mg, 167 mg, 250 mg packets unbuffered enteric coated capsule, 125 mg, 200 mg, 250 mg, 400 mg lamivudine (3TC) tablet, 150 mg oral solution, 50 mg/5 ml stavudine (d4T) capsule 15 mg, 20 mg, 30 mg, 40 mg powder for oral solution, 5 mg/5 ml

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

70 6. Anti-infective medicines (continued) zidovudine (ZDV or AZT) tablet, 300 mg capsule 100 mg, 250 mg oral solution or syrup, 50 mg/ 5ml solution for IV infusion injection, 10 mg/ml in 20-ml vial 6.4.2.2 Non-nucleoside reverse transcriptase inhibitors efavirenz (EFV or EFZ) capsule, 50 mg, 100 mg, 200 mg oral solution, 150 mg/5 ml nevirapine (NVP) tablet, 200 mg oral suspension, 50 mg/5ml 6.4.2.3 Protease inhibitors Selection of two or three protease inhibitors from the Model List will need to be determined by each country after consideration of local treatment guidelines and experience, as well as the comparative costs of available products. Ritonavir is recommended for use in combination with indinavir, lopinavir and saquinavir as a booster, and not as a medicine in its own right. indinavir (IDV) capsule, 200 mg, 333 mg, 400 mg (as sulfate) lopinavir + ritonavir (LPV/r) capsule, 133.3 mg + 33.3 mg oral solution, 400 mg + 100 mg/5 ml nelﬁnavir (NFV) tablet, 250 mg (as mesilate) oral powder, 50 mg/g ritonavir capsule, 100 mg oral solution, 400 mg/5 ml saquinavir (SQV) capsule, 200 mg 6.5 Antiprotozoal medicines 6.5.1 Antiamoebic and antigiardiasis medicines diloxanide tablet, 500 mg (furoate) metronidazole tablet, 200–500 mg injection, 500 mg in 100-ml vial oral suspension, 200 mg (as benzoate)/ 5ml 6.5.2 Antileishmaniasis medicines meglumine antimoniate injection, 30%, equivalent to approximately 8.1% antimony in 5-ml ampoule

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

71 6. Anti-infective medicines (continued) Complementary list amphotericin B powder for injection, 50 mg in vial pentamidine powder for injection, 200 mg, 300 mg (isetionate) in vial 6.5.3 Antimalarial medicines 6.5.3.1 For curative treatment Medicines for the treatment of Plasmodium falciparum malaria cases should be used in combination. amodiaquinea tablet, 153 mg or 200 mg (base) artemether + lumefantrineb tablet, 20 mg + 120 mg chloroquine tablet 100 mg, 150 mg (as phosphate or sulfate) syrup, 50 mg (as phosphate or sulfate)/ 5ml injection, 40 mg (as hydrochloride, phosphate or sulfate)/ml in 5-ml ampoule primaquine tablet, 7.5 mg, 15 mg (as diphosphate) quinine tablet, 300 mg (as bisulfate or sulfate) injection, 300 mg (as dihydrochloride)/ml in 2-ml ampoule Complementary list artemether injection, 80 mg/ml in 1-ml ampoule artesunate tablet, 50 mg doxycycline capsule or tablet, 100 mg (hydrochloride) (for use only in combination with quinine) meﬂoquine tablet, 250 mg (as hydrochloride) sulfadoxine + pyrimethamine tablet, 500 mg + 25 mg 6.5.3.2 For prophylaxis chloroquine tablet, 150 mg (as phosphate or sulfate) syrup, 50 mg (as phosphate or sulfate)/ 5ml

a Amodiaquine should preferably be used as part of combination therapy. b Recommended for use in areas with signiﬁcant drug resistance and not in pregnancy or in children below 10 kg. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

72 6. Anti-infective medicines (continued) doxycycline capsule or tablet, 100 mg (hydrochloride) meﬂoquine tablet, 250 mg (as hydrochloride) proguanila tablet, 100 mg (hydrochloride) 6.5.4 Anti-pneumocystosis and antitoxoplasmosis medicines pyrimethamine tablet, 25 mg sulfamethoxazole + trimethoprim injection, 80 mg + 16 mg/ml in 5-ml ampoule 80 mg + 16 mg/ml in 10-ml ampoule Complementary list pentamidine tablet, 200 mg, 300 mg

6.5.5 Antitrypanosomal medicines

6.5.5.1 African trypanosomiasis melarsoprol injection, 3.6% solution suramin sodium powder for injection, 1 g in vial Complementary list eﬂornithine injection, 200 mg (hydrochloride)/ml in 100-ml bottle pentamidine powder for injection, 200 mg, 300 mg (isetionate) in vial 6.5.5.2 American trypanosomiasis benznidazole tablet, 100 mg nifurtimox tablet, 30 mg, 120 mg, 250 mg

7. Antimigraine medicines 7.1 For treatment of acute attack acetylsalicylic acid tablet, 300–500 mg paracetamol tablet, 300–500 mg

7.2 For prophylaxis propranolol tablet, 20 mg, 40 mg (hydrochloride)

a For use only in combination with chloroquine. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

73 8. Antineoplastic, immunosuppressives and medicines used in palliative care 8.1 Immunosuppressive medicines Complementary list azathioprine tablet, 50 mg powder for injection, 100 mg (as sodium salt) in vial ciclosporin capsule, 25 mg concentrate for injection, 50 mg/ml in 1-ml ampoule for organ transplantation 8.2 Cytotoxic medicines Complementary list asparaginase powder for injection, 10 000 IU in vial bleomycin powder for injection, 15 mg (as sulfate) in vial calcium folinate tablet, 15 mg injection, 3 mg/ml in 10-ml ampoule chlorambucil tablet, 2 mg chlormethine powder for injection, 10 mg (hydrochloride) in vial cisplatin powder for injection, 10 mg, 50 mg in vial cyclophosphamide tablet, 25 mg powder for injection, 500 mg in vial cytarabine powder for injection, 100 mg in vial dacarbazine powder for injection, 100 mg in vial dactinomycin powder for injection, 500 micrograms in vial daunorubicin powder for injection, 50 mg (as hydrochloride) doxorubicin powder for injection, 10 mg, 50 mg (hydrochloride) in vial etoposide capsule, 100 mg injection, 20 mg/ml in 5-ml ampoule ﬂuorouracil injection, 50 mg/ml in 5-ml ampoule levamisole tablet, 50 mg (as hydrochloride) mercaptopurine tablet, 50 mg

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

74 8. Antineoplastic, immunosuppressives and medicines used in palliative care (continued) methotrexate tablet, 2.5 mg (as sodium salt) powder for injection, 50 mg (as sodium salt) in vial procarbazine capsule, 50 mg (as hydrochloride) vinblastine powder for injection, 10 mg (sulfate) in vial vincristine powder for injection, 1 mg, 5 mg (sulfate) in vial 8.3 Hormones and antihormones Complementary list dexamethasone injection, 4 mg dexamethasone phosphate (as disodium salt) in 1-ml ampoule hydrocortisone powder for injection, 100 mg (as sodium succinate) in vial prednisolonea tablet, 5 mg, 25 mg tamoxifen tablet, 10 mg, 20 mg (as citrate) 8.4 Medicines used in palliative care The WHO Expert Committee on the Selection and Use of Essential Medicines recommended that all the medicines mentioned in the WHO publication Cancer pain relief: with a guide to opioid availability, 2nd ed., be considered essential (1). The medicines are included in the relevant sections of the Model List, according to their therapeutic use, e.g. as analgesics.

9. Antiparkinsonism medicines biperiden tablet, 2 mg (hydrochloride) injection, 5 mg (lactate) in 1-ml ampoule levodopa + carbidopa tablet, 100 mg + 10 mg; 250 mg + 25 mg

10. Medicines affecting the blood 10.1 Antianaemia medicines ferrous salt tablet, equivalent to 60 mg iron oral solution, equivalent to 25 mg iron (as sulfate)/ml ferrous salt + folic acidb tablet, equivalent to 60 mg iron + 400 micrograms folic acid

a There is no evidence for complete clinical similarity between prednisolone and dexamethasone at high doses. b Nutritional supplement for use during pregnancy. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

75 10. Medicines affecting the blood (continued) folic acid tablet, 1 mg, 5 mg hydroxocobalamin injection, 1 mg in 1-ml ampoule 10.2 Medicines affecting coagulation heparin sodium injection, 1000 IU/ml, 5000 IU/ml, 20 000 IU/ml in 1-ml ampoule phytomenadione injection, 10 mg/ml in 5-ml ampoule tablet, 10 mg protamine sulfate injection, 10 mg/ml in 5-ml ampoule warfarin tablet, 1 mg, 2 mg, 5 mg (sodium salt)

11. Blood products and plasma substitutes 11.1 Plasma substitutes dextran 70a injectable solution, 6% 11.2 Plasma fractions for speciﬁc use All plasma fractions should comply with the Requirements for the collection, processing and quality control of blood, blood components, and plasma derivatives (Revised 1992) as published in the forty-third report of the WHO Expert Committee on Biological Standardization (2). Complementary list factor VIII concentrate dried factor IX complex (coagulation dried factors, II, VII, IX, X) concentrate

12. Cardiovascular medicines 12.1 Antianginal medicines atenolol tablet, 50 mg, 100 mg glyceryl trinitrate tablet (sublingual), 500 micrograms isosorbide dinitrate tablet (sublingual), 5 mg verapamil tablet, 40 mg, 80 mg (hydrochloride) 12.2 Antiarrhythmic medicines This subsection will be reviewed at the next meeting of the Expert Committee when it is anticipated that applications for amiodarone and sotalol will be received.

a Polygeline, injectable solution, 3.5% is considered as equivalent. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

76 12. Cardiovascular medicines (continued) atenolol tablet, 50 mg, 100 mg digoxin tablet, 62.5 micrograms, 250 micrograms oral solution, 50 micrograms/ml injection, 250 micrograms/ml in 2-ml ampoule epinephrine (adrenaline) injection, 1 mg (as hydrochloride)/ml in ampoule lidocaine injection, 20 mg (hydrochloride)/ml in 5-ml ampoule verapamil tablet, 40 mg, 80 mg (hydrochloride) injection, 2.5 mg (hydrochloride)/ml in 2-ml ampoule Complementary list procainamide injection, 100 mg (hydrochloride)/ml in 10-ml ampoule quinidine tablet, 200 mg (sulfate) 12.3 Antihypertensive medicines amlodipine tablet, 5 mg atenolol tablet, 50 mg, 100 mg enalapril tablet, 2.5 mg hydralazinea tablet, 25 mg, 50 mg (hydrochloride) powder for injection, 20 mg (hydrochloride) in ampoule hydrochlorothiazide scored tablet, 25 mg methyldopab tablet, 250 mg Complementary list sodium nitroprusside powder for infusion, 50 mg in ampoule

a Hydralazine is listed for use in the acute management of severe pregnancy-induced hypertension only. Its use in the treatment of essential hypertension is not recommended in view of the availability of more evidence of efﬁcacy and safety of other medicines. b Methyldopa is listed for use in the management of pregnancy-induced hypertension only. Its use in the treatment of essential hypertension is not recommended in view of the availability of more evidence of efﬁcacy and safety of other medicines. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

77 12. Cardiovascular medicines (continued) 12.4 Medicines used in heart failure This subsection will be reviewed at the next meeting of the Expert Committee. digoxin tablet, 62.5 micrograms, 250 micrograms oral solution, 50 micrograms/ml injection, 250 micrograms/ml in 2-ml ampoule enalapril tablet, 2.5 mg furosemide tablet, 40 mg injection, 10 mg/ml in 2-ml ampoule hydrochlorothiazide scored tablet, 25 mg Complementary list dopamine injection, 40 mg (hydrochloride) in 5-ml vial 12.5 Antithrombotic medicines acetylsalicylic acid tablet, 100 mg Complementary list streptokinase powder for injection, 1.5 million IU in vial 12.6 Lipid-lowering agents The WHO Expert Committee on the Selection and Use of Essential Medicines recognizes the value of lipid-lowering medicines in treating patients with hyperlipidaemia. β-Hydroxy-β-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, often referred to as “statins”, are a family of potent and effective lipid- lowering medicines with a good tolerability proﬁle. Several of these medicines have been shown to reduce the incidence of fatal and non-fatal myocardial infarction, stroke and mortality (all causes), as well as the need for coronary by- pass surgery. All remain very costly but may be cost-effective for secondary prevention of cardiovascular disease as well as for primary prevention in some very high-risk patients. Since no single medicine has been shown to be signiﬁcantly more effective or less expensive than others in the group, none is included in the Model List; the choice of medicine for use in patients at highest risk should be decided at the national level.

13. Dermatological medicines (topical) 13.1 Antifungal medicines benzoic acid + salicylic acid ointment or cream, 6% + 3% miconazole ointment or cream, 2% (nitrate) sodium thiosulfate solution, 15%

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

78 13. Dermatological medicines (topical) (continued) 13.2 Anti-infective medicines Complementary list selenium sulfide detergent-based suspension, 2% methylrosanilinium aqueous solution, 0.5% chloride (gentian violet) tincture, 0.5% neomycin sulfate + bacitracin ointment, 5 mg neomycin sulfate + 500 IU bacitracin zinc/g potassium permanganate aqueous solution, 1 : 10 000 silver sulfadiazine cream, 1%, in 500-g container 13.3 Anti-inflammatory and antipruritic medicines betamethasone ointment or cream, 0.1% (as valerate) calamine lotion lotion hydrocortisone ointment or cream, 1% (acetate) 13.4 Astringent medicines aluminium diacetate solution, 13% for dilution 13.5 Medicines affecting skin differentiation and proliferation benzoyl peroxide lotion or cream, 5% coal tar solution, 5% dithranol ointment, 0.1%–2% fluorouracil ointment, 5% podophyllum resin solution, 10–25% salicylic acid solution, 5% urea ointment or cream, 10% 13.6 Scabicides and pediculicides benzyl benzoate lotion, 25% permethrin cream, 5% lotion, 1%

14. Diagnostic agents 14.1 Ophthalmic medicines ﬂuorescein eye drops, 1% (sodium salt) tropicamide eye drops, 0.5%

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

79 14. Diagnostic agents (continued) 14.2 Radiocontrast media amidotrizoate injection, 140–420 mg iodine (as sodium or meglumine salt)/ml in 20-ml ampoule barium sulfate aqueous suspension iohexol injection, 140–350 mg iodine/ml in 5-ml, 10-ml or 20-ml ampoule iopanoic acid tablet, 500 mg propyliodone oily suspension, 500–600 mg/ml in 20-ml ampoulea Complementary list meglumine iotroxate solution, 5–8 g iodine in 100–250 ml

15. Disinfectants and antiseptics 15.1 Antiseptics chlorhexidine solution, 5% (digluconate) for dilution ethanol solution, 70% (denatured) polyvidone iodine solution, 10% 15.2 Disinfectants chlorine base compound powder (0.1% available chlorine) for solution chloroxylenol solution, 4.8% glutaral solution, 2%

16. Diuretics amiloride tablet, 5 mg (hydrochloride) furosemide tablet, 40 mg injection, 10 mg/ml in 2-ml ampoule hydrochlorothiazide scored tablet, 25 mg mannitol injectable solution, 10%, 20% spironolactone tablet, 25 mg

17. Gastrointestinal medicines 17.1 Antacids and other antiulcer medicines aluminium hydroxide tablet, 500 mg oral suspension, 320 mg/5 ml

a For administration only into the bronchial tree. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

80 17. Gastrointestinal medicines (continued) magnesium hydroxide oral suspension, equivalent to 550 mg magnesium oxide/10 ml ranitidine tablet, 150 mg (as hydrochloride) oral solution, 75 mg/5ml injection, 25 mg/ml in 2-ml ampoule 17.2 Antiemetic medicines metoclopramide tablet, 10 mg (hydrochloride) injection, 5 mg (hydrochloride)/ml in 2-ml ampoule promethazine tablet, 10 mg, 25 mg (hydrochloride) elixir or syrup, 5 mg (hydrochloride)/5 ml injection, 25 mg (hydrochloride)/ml in 2-ml ampoule 17.3 Anti-inﬂammatory medicines sulfasalazine tablet, 500 mg suppository, 500 mg retention enema Complementary list hydrocortisonea suppository, 25 mg (acetate) retention enema 17.4 Laxatives senna tablet, 7.5 mg (sennosides) (or traditional dosage forms) 17.5 Medicines used in diarrhoea 17.5.1 Oral rehydration oral rehydration salts (for glucose– powder, 20.5 g/l electrolyte solution) Components (for 1 litre of glucose– electrolyte solution)b glucose: 13.5 g/l sodium chloride: 2.6 g/l potassium chloride: 1.5 g/l

a The square box symbol () only applies to hydrocortisone retention enema. b In cases of cholera a higher concentration of sodium may be required. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

81 17. Gastrointestinal medicines (continued) trisodium citrate dihydratea: 2.9 g/l These components provide a glucose– electrolyte solution with the following molar concentrations: glucose: 75 mEq sodium: 75 mEq or mmol/l chloride: 65 mEq or mmol/l potassium: 20 mEq or mmol/l citrate: 10 mmol/l osmolarity: 245 mOsm/l

17.5.2 Medicines for diarrhoea in children zinc sulfateb tablet or syrup in 10 mg per unit dosage forms

17.5.3 Antidiarrhoeal (symptomatic) medicines for adults codeinec tablet, 30 mg (phosphate)

18. Hormones, other endocrine medicines and contraceptives 18.1 Adrenal hormones and synthetic substitutes Addison disease is a rare condition; adrenal hormones for the treatment of this condition are already included in section 3.

18.2 Androgens Complementary list testosterone injection, 200 mg (enantate) in 1-ml ampoule

18.3 Contraceptives This subsection will be reviewed at the next meeting of the Expert Committee. 18.3.1 Oral hormonal contraceptives ethinylestradiol + levonorgestrel tablet, 30 micrograms + 150 micrograms

a Trisodium citrate dihydrate may be replaced by sodium hydrogen carbonate (sodium bicarbonate) 2.5 g/l. However, as the stability of this latter formulation is very poor under tropical conditions, it is only recommended when manufactured for immediate use. b In acute diarrhoea, zinc sulfate should be used as an adjunct to oral rehydration salts. c The therapeutic efﬁcacy of this item has been questioned and its continued inclusion on the list will be reviewed at the next meeting of the Expert Committee. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

82 18. Hormones, other endocrine medicines and contraceptives (continued) ethinylestradiol + norethisterone tablet, 35 micrograms + 1.0 mg levonorgestrel tablet, 30 micrograms, 750 micrograms (pack of two), 1.5 mg 18.3.2 Injectable hormonal contraceptives medroxyprogesterone acetate depot injection, 150 mg/ml in 1-ml vial norethisterone enantate oily solution, 200 mg/ml in 1-ml ampoule 18.3.3 Intrauterine devices copper-containing device 18.3.4 Barrier methods condoms diaphragms 18.4 Estrogens ethinylestradiola tablet, 10 micrograms, 50 micrograms 18.5 Insulins and other antidiabetic agents glibenclamide tablet, 2.5 mg, 5 mg insulin injection (soluble) injection, 40 IU/ml in 10-ml vial, 100 IU/ml in 10-ml vial intermediate-acting insulin injection, 40 IU/ml in 10-ml vial 100 IU/ml in 10-ml vial (as compound insulin zinc suspension or isophane insulin) metformin tablet, 500 mg (hydrochloride) 18.6 Ovulation inducers Complementary list clomifene tablet, 50 mg (citrate) 18.7 Progestogens norethisteronea tablet, 5 mg

a The public health relevance and/or comparative efﬁcacy and/or safety of this item has been questioned and its continued inclusion on the Model List will be reviewed at the next meeting of the Expert Committee. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

83 18. Hormones, other endocrine medicines and contraceptives (continued) Complementary list medroxyprogesterone tablet, 5 mg acetatea 18.8 Thyroid hormones and antithyroid medicines levothyroxine tablet, 50 micrograms, 100 micrograms (sodium salt) potassium iodide tablet, 60 mg propylthiouracil tablet, 50 mg 19. Immunologicals 19.1 Diagnostic agents All tuberculins should comply with the WHO Requirements for Tuberculins (Revised 1985). WHO Expert Committee on Biological Standardization, Thirty- sixth report (WHO Technical Report Series, No. 745, 1987, Annex 1) (3). tuberculin, puriﬁed injection protein derivative (PPD) 19.2 Sera and immunoglobulins All plasma fractions should comply with the WHO Requirements for the Collection, Processing and Quality Control of Blood, Blood Components and Plasma Derivatives (Revised 1992). WHO Expert Committee on Biological Standardization, Forty-third report (WHO Technical Report Series, No. 840, 1994, Annex 2) (2). anti-D immunoglobulin (human) injection, 250 micrograms in single-dose vial antitetanus immunoglobulin injection, 500 IU in vial (human) antivenom serumb injection diphtheria antitoxin injection, 10 000 IU, 20 000 IU in vial rabies immunoglobulin injection, 150 IU/ml in vial 19.3 Vaccines All vaccines should comply with the WHO requirements for biological substances, as published in the reports of the WHO Expert Committee on Biological Standardization. BCG vaccines should comply with the Requirements for Dried BCG Vaccine (Revised 1985), as published in the thirty-sixth report of the WHO

a The public health relevance and/or comparative efﬁcacy and/or safety of this item has been questioned and its continued inclusion on the list will be reviewed at the next meeting of the Expert Committee. b Exact type to be deﬁned locally. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

84 19. Immunologicals (continued) Expert Committee on Biological Standardization (4) and subsequent Amend- ment 1987 as published in the thirty-eighth report of the WHO Expert Committee on Biological Standardization (5). Diphtheria, pertussis and tetanus vaccines should comply with the Requirements for Diphtheria, Tetanus, Pertussis and Combined Vaccines (Revised 1989), as published in the fortieth report of the WHO Expert Committee on Biological Standardization (6). Hepatitis B vaccines should comply with the Requirements for Hepatitis B Vaccine Prepared from Plasma (Revised 1994), as published in the forty-fifth report of the WHO Expert Committee on Biological Standardization (7). Measles, mumps and rubella vaccines should comply with the Requirements for Measles, Mumps and Rubella Vaccines and Combined Vaccine (Live) (Revised 1992), as published in the forty-third report of the WHO Expert Committee on Biological Standardization (8) and subsequent Note, as published in the forty-fourth report of the WHO Expert Committee on Biological Standardization (9). Poliomyelitis vaccines should comply with the Requirements for Poliomyelitis Vaccine (Oral) (Revised 1989) as published in the fortieth report of the WHO Expert Committee on Biological Standardization (10) or the Requirements for Poliomyelitis Vaccine (Inactivated) (Revised 1981), as published in the report of the WHO Expert Committee on Biological Standardization (11) and subsequent Addendum 1985, as published in the thirty-sixth report of the WHO Expert Committee on Biologi- cal Standardization (12). Influenza vaccines should comply with the Require- ments for Influenza Vaccine (Inactivated) (Revised 1990), as published in the forty-first report of the WHO Expert Committee on Biological Standardization (13). Meningococcal meningitis vaccines should comply with the Requirements for Meningococcal Polysaccharide Vaccine, as published in the report of the WHO Expert Committee on Biological Standardization (14) and subsequent Addendum 1980, incorporating Addendum 1976 and Addendum 1977, as published in the thirty-first report of the WHO Expert Committee on Biological Standardization (15). Rabies vaccines should comply with the Requirements for Rabies Vaccine for Human Use (Revised 1980), as published in the thirty-first report of the WHO Expert Committee on Biological Standardization (16) and subsequent Amendment 1992, as published in the forty-third report of the WHO Expert Committee on Biological Standardization (17), or the Requirements for Rabies Vaccine (Inactivated) for Human Use Produced in Continuous Cell Lines (Revised 1986), as published in the thirty-seventh report of the WHO Expert Committee on Biological Standardization (18) and subsequent Amendment 1992, as published in the forty-third report of the WHO Expert Committee on Biological Standardization (19). Typhoid vaccines should comply with the Requirements for Typhoid Vaccine (Live, Attenuated, Ty 21s, Oral), as published in the report of the WHO Expert Committee on Biological Standardization (20) or the Requirements for Vi Polysaccharide Typhoid Vaccine, as published in the forty-third report of the WHO Expert Committee on Biological Standardization (21). Yellow fever vaccines should comply with Requirements for Yellow Fever Vaccine (Revised 1995), as published in the forty-sixth report of the WHO Expert Committee on Biological Standardization (22).

85 19. Immunologicals (continued) 19.3.1 For universal immunization BCG vaccine diphtheria vaccine hepatitis B vaccine measles vaccine pertussis vaccine poliomyelitis vaccine tetanus vaccine 19.3.2 For speciﬁc groups of individuals inﬂuenza vaccine meningococcal meningitis vaccine mumps vaccine rabies vaccine (inactivated: prepared in cell culture) rubella vaccine typhoid vaccine yellow fever vaccine

20. Muscle relaxants (peripherally-acting) and cholinesterase inhibitors alcuroniuma injection, 5 mg (chloride)/ml in 2-ml ampoule neostigmine tablet, 15 mg (bromide) injection, 500 micrograms in 1-ml ampoule 2.5 mg (metilsulfate) in 1-ml ampoule suxamethonium injection, 50 mg (chloride)/ml in 2-ml ampoule powder for injection (chloride), in vial Complementary list pyridostigmine tablet, 60 mg (bromide) injection, 1 mg in 1-ml ampoule

a It is likely that alcuronium will be replaced and that similar products, including atracurium and/or pancuronium will be added at the next meeting of the Expert Committee. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

86 20. Muscle relaxants (peripherally-acting) and cholinesterase inhibitors (continued) vecuronium powder for injection, 10 mg (bromide) in vial

21. Ophthalmological preparations This section will be reviewed at the next meeting of the Expert Committee. 21.1 Anti-infective agents gentamicina solution (eye drops), 0.3% (sulfate) idoxuridine solution (eye drops), 0.1% eye ointment, 0.2% tetracycline eye ointment, 1% (hydrochloride) 21.2 Anti-inﬂammatory agents prednisolone solution (eye drops), 0.5% (sodium phosphate) 21.3 Local anaesthetics tetracaine solution (eye drops), 0.5% (hydrochloride) 21.4 Miotics and antiglaucoma medicines acetazolamide tablet, 250 mg pilocarpine solution (eye drops), 2%, 4% (hydrochloride or nitrate) timolol solution (eye drops), 0.25%, 0.5% (as maleate) 21.5 Mydriatics atropine solution (eye drops), 0.1%, 0.5%, 1% (sulfate) Complementary list epinephrine (adrenaline) solution (eye drops), 2% (as hydrochloride)

22. Oxytocics and antioxytocics 22.1 Oxytocics ergometrine injection, 200 micrograms (hydrogen maleate) in 1-ml ampoule oxytocin injection, 10 IU in 1-ml ampoule Complementary list misoprostol vaginal tablet, 25 micrograms

a Final selection depends on indication for use. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

87 22. Oxytocics and antioxytocics (continued) mifepristonea — misoprostola tablet, 200 mg — tablet, 200 micrograms Where permitted under national law and where culturally acceptable.

22.2 Antioxytocics nifedipine immediate release capsule, 10 mg

23. Peritoneal dialysis solution Complementary list intraperitoneal dialysis parenteral solution solution (of appropriate composition)

24. Psychotherapeutic medicines 24.1 Medicines used in psychotic disorders chlorpromazine tablet, 100 mg (hydrochloride)

syrup, 25 mg (hydrochloride)/5 ml injection, 25 mg (hydrochloride)/ml in 2-ml ampoule ﬂuphenazine injection, 25 mg (decanoate or enantate) in 1-ml ampoule haloperidol tablet, 2 mg, 5 mg injection, 5 mg in 1-ml ampoule 24.2 Medicines used in mood disorders 24.2.1 Medicines used in depressive disorders amitriptyline tablet, 25 mg (hydrochloride) 24.2.2 Medicines used in bipolar disorders carbamazepine scored tablet, 100 mg, 200 mg lithium carbonate capsule or tablet, 300 mg valproic acid enteric coated tablet, 200 mg, 500 mg (sodium salt) 24.3 Medicines used in generalized anxiety and sleep disorders diazepam scored tablet, 2 mg, 5 mg 24.4 Medicines used for obsessive–compulsive disorders and panic attacks clomipramine capsules, 10 mg, 25 mg (hydrochloride) a Requires close medical supervision. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

88 24. Psychotherapeutic medicines (continued) 24.5 Medicines used in substance dependence programmes Complementary list methadonea oral solution, 5 mg/5 ml, 10 mg/5 ml concentrate for oral solution, 5 mg/ml, 10 mg/ml (hydrochloride)

25. Medicines acting on the respiratory tract 25.1 Antiasthmatic and medicines for chronic obstructive pulmonary disease beclometasone inhalation (aerosol), 50 micrograms per dose (dipropionate) 250 micrograms (dipropionate) per dose epinephrine (adrenaline) injection, 1 mg (as hydrochloride or hydrogen tartrate) in 1-ml ampoule ipratropium bromide inhalation (aerosol), 20 micrograms/ metered dose salbutamol tablet, 2 mg, 4 mg (as sulfate) inhalation (aerosol), 100 micrograms (as sulfate) per dose syrup, 2 mg (as sulfate)/5 ml injection, 50 micrograms (as sulfate)/ml in 5-ml ampoule respirator solution for use in nebulizers, 5 mg (as sulfate)/ml

26. Solutions correcting water, electrolyte and acid–base disturbances 26.1 Oral oral rehydration salts (for glucose– For composition see section 17.5.1 electrolyte solution) potassium chloride powder for solution 26.2 Parenteral glucose injectable solution, 5%, 10% isotonic, 50% hypertonic glucose with sodium chloride injectable solution, 4% glucose, 0.18% sodium chloride (equivalent to Na+ 30 mmol/l, Cl− 30 mmol/l)

a The square box is added to include buprenorphine. The medicines should be used only within an established support programme. Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

89 26. Solutions correcting water, electrolyte and acid-base disturbances (continued) potassium chloride solution, 11.2% in 20-ml ampoule (equivalent to K+ 1.5 mmol/ml, Cl− 1.5 mmol/ml) sodium chloride injectable solution, 0.9% isotonic (equivalent to Na+ 154 mmol/l, Cl− 154 mmol/l sodium hydrogen carbonate injectable solution, 1.4% isotonic + − (equivalent to Na 167 mmol/l, HCO3 167 mmol/l) solution, 8.4% in 10-ml ampoule + − (equivalent to Na 1000 mmol/l, HCO3 1000 mmol/l) sodium lactate, solution compound injectable solution 26.3 Miscellaneous water for injection 2-ml, 5-ml, 10-ml ampoules

27. Vitamins and minerals ascorbic acid tablet, 50 mg ergocalciferol capsule or tablet, 1.25 mg (50 000 IU); oral solution, 250 micrograms/ml (10 000 IU/ml) iodine iodized oil, 1 ml (480 mg iodine), 0.5 ml (240 mg iodine) in ampoule (oral or injectable) 0.57 ml (308 mg iodine) in dispenser bottle capsule, 200 mg nicotinamide tablet, 50 mg pyridoxine tablet, 25 mg (hydrochloride) retinol sugar-coated tablet, 10 000 IU (as palmitate) (5.5 mg) capsule, 200 000 IU (as palmitate) (110 mg) oral oily solution, 100 000 IU (as palmitate)/ml in multidose dispenser water-miscible injection, 100 000 IU (as palmitate) (55 mg) in 2-ml ampoule riboﬂavin tablet, 5 mg

Recommended example within a pharmaceutical class. See Explanatory notes on page 61.

90 27. Vitamins and minerals (continued) sodium ﬂuoride in any appropriate topical formulation thiamine tablet, 50 mg (hydrochloride) Complementary list calcium gluconate injection, 100 mg/ml in 10-ml ampoule

References

1. Cancer pain relief with a guide to opioid availability. 2nd ed. Geneva, World Health Organization, 1996. 2. Requirements for the Collection, Processing and Quality Control of Blood, Blood Components, and Plasma Derivatives (Revised 1992). In: WHO Expert Committee on Biological Standardization. Forty-third report. Geneva, World Health Organization, 1994, Annex 2 (WHO Technical Report Series, No. 840). 3. Requirements for Tuberculins (Revised 1985). In: WHO Expert Committee on Biological Standardization. Thirty-sixth report. Geneva, World Health Organization, 1987, Annex 1 (WHO Technical Report Series, No. 745). 4. Requirements for Dried BCG Vaccine (Revised 1985). In: WHO Expert Committee on Biological Standardization. Thirty-sixth report. Geneva, World Health Organization, 1987, Annex 2 (WHO Technical Report Series, No. 745). 5. Requirements for Dried BCG Vaccine (Amendment 1987). In: WHO Expert Committee on Biological Standardization. Thirty-eighth report. Geneva, World Health Organization, 1988, Annex 12 (WHO Technical Report Series, No. 771). 6. Requirements for Diphtheria, Tetanus, Pertussis and Combined Vaccines (Revised 1989). In: WHO Expert Committee on Biological Standardization. Fortieth report. Geneva, World Health Organization, 1990, Annex 2 (WHO Technical Report Series, No. 800). 7. Requirements for Hepatitis B Vaccine Prepared from Plasma (Revised 1994). In: WHO Expert Committee on Biological Standardization. Forty-ﬁfth report. Geneva, World Health Organization, 1995, Annex 3 (WHO Technical Report Series, No. 858). 8. Requirements for Measles, Mumps and Rubella Vaccines and Combined Vaccine (Live) (Revised 1992). In: WHO Expert Committee on Biological Standardization. Forty-third report. Geneva, World Health Organization, 1994, Annex 3 (WHO Technical Report Series, No. 840). 9. Requirements for Measles, Mumps and Rubella Vaccines and Combined Vaccine (Live). In: WHO Expert Committee on Biological Standardization. Forty-fourth report. Geneva, World Health Organization, 1994, Note (WHO Technical Report Series, No. 848). 10. Requirements for Poliomyelitis Vaccine (Oral) (Revised 1989). In: WHO Expert Committee on Biological Standardization. Fortieth report. Geneva,

91 World Health Organization, 1990, Annex 1 (WHO Technical Report Series, No. 800). 11. Requirements for Poliomyelitis Vaccine (Inactivated) (Revised 1981). In: WHO Expert Committee on Biological Standardization. Fortieth report. Geneva, World Health Organization, 1982, Annex 2 (WHO Technical Report Series, No. 673). 12. Requirements for Poliomyelitis Vaccine (Inactivated) (Addendum 1985). In: WHO Expert Committee on Biological Standardization Thirty-sixth report. Geneva, World Health Organization, 1987, Annex 4 (WHO Technical Report Series, No. 745). 13. Requirements for Influenza Vaccine (Inactivated) (Revised 1990). In: WHO Expert Committee on Biological Standardization. Forty-first report. Geneva, World Health Organization, 1991, Annex 2 (WHO Technical Report Series, No. 814). 14. Requirements for Meningococcal Polysaccharide Vaccine. In: WHO Expert Committee on Biological Standardization. Geneva, World Health Organization, 1976, Annex 2 (WHO Technical Report Series, No. 594). 15. Requirements for Meningococcal Polysaccharide Vaccine (Addendum 1980, incorporating Addendum 1976 and Addendum 1977). In: WHO Expert Committee on Biological Standardization. Thirty-first report. Geneva, World Health Organization, 1981, Annex 6 (WHO Technical Report Series, No. 658). 16. Requirements for Rabies Vaccine for Human Use (Revised 1980). In: WHO Expert Committee on Biological Standardization. Thirty-first report. Geneva, World Health Organization, 1981, Annex 2 (WHO Technical Report Series, No. 658). 17. Requirements for Rabies Vaccine for Human Use (Amendment 1992). In: WHO Expert Committee on Biological Standardization. Forty-third report. Geneva, World Health Organization, 1994, Annex 4 (WHO Technical Report Series, No. 840). 18. Requirements for Rabies Vaccine (Inactivated) for Human Use Produced in Continuous Cell Lines (Revised 1986). In: WHO Expert Committee on Biological Standardization. Thirty-seventh report. Geneva, World Health Organization, 1987, Annex 9 (WHO Technical Report Series, No. 760). 19. Requirements for Rabies Vaccine (Inactivated) for Human Use Produced in Continuous Cell Lines (Amendment 1992). In: WHO Expert Committee on Biological Standardization. Forty-third report. Geneva, World Health Organization, 1994, Annex 5 (WHO Technical Report Series, No. 840). 20. Requirements for Typhoid Vaccine (Live, Attenuated, Ty 21a, Oral) In: WHO Expert Committee on Biological Standardization. Geneva, World Health Organization, 1984, Annex 3 (WHO Technical Report Series, No. 700). 21. Requirements for Vi Polysaccharide Typhoid Vaccine. In: WHO Expert Committee on Biological Standardization. Forty-third report. Geneva, World Health Organization, 1994, Annex 1 (WHO Technical Report Series, No. 840). 22. Requirements for Yellow Fever Vaccine (Revised 1995). In: WHO Expert Committee on Biological Standardization. Forty-sixth report. Geneva, World Health Organization, 1998, Annex 2 (WHO Technical Report Series, No. 872).

92 © World Health Organization WHO Technical Report Series, No. 933, 2006

Annex 2 The Anatomical Therapeutic Chemical (ATC) classiﬁcation system1

The following list provides the corresponding Anatomical Thera- peutic Chemical (ATC) classiﬁcation codes for all items on the 14th WHO Model List of Essential Medicines, sorted by ATC code number.

ATC code ATC group/medicine or item

A ALIMENTARY TRACT AND METABOLISM A02 Drugs for acid related disorders A02A Antacids A02AA Magnesium compounds A02AA04 magnesium hydroxide A02AB Aluminium compounds A02AB01 aluminium hydroxide A02B Drugs for peptic ulcer and gastro-oesophageal reﬂux disease (GORD)

A02BA H2-receptor antagonists A02BA02 ranitidine A02BB Prostaglandins A02BB01 misoprostol A03 Drugs for functional gastrointestinal disorders A03B Belladonna and derivatives, plain A03BA Belladonna alkaloids, tertiary amines A03BA01 atropine A03F Propulsives A03FA Propulsives A03FA01 metoclopramide A06 Laxatives A06A Laxatives A06AB Contact laxatives A06AB06 senna*

1 Based on the ATC list as of January 2005 and prepared with the assisance of the WHO Collaborating Centre for Drug Statistics Methodology, Oslo, Norway.

93 ATC code ATC group/medicine or item

A07 Antidiarrheals, intestinal antiinﬂammatory/antiinfective agents A07A Intestinal antiinfectives A07AA Antibiotics A07AA02 nystatin

A07B Intestinal adsorbents A07BA Charcoal preparations A07BA01 charcoal, activated*

A07C Electrolytes with carbohydrates A07CA oral rehydration salts*

A07E Intestinal antiinﬂammatory agents A07EA Corticosteroids for local use A07EA02 hydrocortisone

A07EC Aminosalicylic acid and similar agents A07EC01 sulfasalazine

A10 Drugs used in diabetes A10A Insulins and analogues A10AB insulin injection (soluble)* A10AC insulin, intermediate-acting*

A10B Oral blood glucose lowering drugs A10BA Biguanides A10BA02 metformin

A10BB Sulfonamides, urea derivatives A10BB01 glibenclamide

A11 Vitamins A11C Vitamin A and D, incl. combinations of the two A11CA Vitamin A, plain A11CA01 retinol

A11CC Vitamin D and analogues A11CC01 ergocalciferol

A11D Vitamin B1, plain and in combination with vitamin B6 and B12

A11DA Vitamin B1, plain A11DA01 thiamine A11G Ascorbic acid (vitamin C), incl. combinations A11GA Ascorbic acid (vitamin C), plain A11GA01 ascorbic acid A11H Other plain vitamin preparations A11HA Other plain vitamin preparations A11HA01 nicotinamide

94 ATC code ATC group/medicine or item

A11HA02 pyridoxine A11HA04 riboﬂavin

A12 Mineral supplements A12A Calcium A12AA Calcium A12AA03 calcium gluconate

A12C Other mineral supplements A12CB Zinc A12CB01 zinc sulfate

A12CD Fluoride A12CD01 sodium ﬂuoride

A12CX Other mineral products A12CX iodine*

B BLOOD AND BLOOD FORMING ORGANS B01 Antithrombotic agents B01A Antithrombotic agents B01AA Vitamin K antagonists B01AA03 warfarin

B01AB Heparin group B01AB01 heparin sodium*

B01AC Platelet aggregation inhibitors excl. heparin B01AC06 acetylsalicylic acid

B01AD Enzymes B01AD01 streptokinase

B02 Antihemorrhagics B02B Vitamin K and other hemostatics B02BA Vitamin K B02BA01 phytomenadione

B02BD Blood coagulation factors B02BD01 factor IX complex (coagulation factors II, VII, IX, X) concentrate* B02BD02 factor VIII concentrate*

B03 Antianemic preparations B03A Iron preparations B03A ferrous salt*

B03AD ferrous salt + folic acid*

B03B Vitamin B12 and folic acid

B03BA Vitamin B12 (cyanocobalamin and analogues) B03BA03 hydroxocobalamin

95 ATC code ATC group/medicine or item

B03BB Folic acid and derivatives B03BB01 folic acid

B05 Blood substitutes and perfusion solutions B05A Blood and related products B05AA Blood substitutes and plasma protein fractions B05AA05 dextran 70* B05AA06 polygeline*

B05B I.v. solutions B05BA Solutions for parenteral nutrition

B05BB Solutions affecting the electrolyte balance B05BB01 sodium lactate, compound solution* B05BB02 glucose with sodium chloride*

B05BC Solutions producing osmotic diuresis B05BC01 mannitol

B05D Peritoneal dialytics B05DA intraperitoneal dialysis solution*

B05X I.v. solution additives B05XA Electrolyte solutions B05XA01 potassium chloride B05XA02 sodium hydrogen carbonate* B05XA03 sodium chloride B05XA05 magnesium sulfate

C CARDIOVASCULAR SYSTEM C01 Cardiac therapy C01A Cardiac glycosides C01AA Digitalis glycosides C01AA05 digoxin

C01B Antiarrhythmics, class I and III C01BA Antiarrhythmics, class Ia C01BA01 quinidine C01BA02 procainamide

C01BB Antiarrhythmics, class Ib C01BB01 lidocaine

C01C Cardiac stimulants excl. cardiac glycosides C01CA Adrenergic and dopaminergic agents C01CA04 dopamine C01CA24 epinephrine

C01D Vasodilators used in cardiac diseases C01DA Organic nitrates C01DA02 glyceryl trinitrate C01DA08 isosorbide dinitrate

96 ATC code ATC group/medicine or item

C02 Antihypertensives C02A Antiadrenergic agents, centrally acting C02AB Methyldopa C02AB01 methyldopa* C02D Arteriolar smooth muscle, agents acting on C02DD Nitroferricyanide derivatives C02DD01 sodium nitroprusside* C03 Diuretics C03A Low-ceiling diuretics, thiazides C03AA Thiazides, plain C03AA03 hydrochlorothiazide C03C High-ceiling diuretics C03CA Sulfonamides, plain C03CA01 furosemide C03D Potassium-sparing agents C03DA Aldosterone antagonists C03DA01 spironolactone C03DB Other potassium-sparing agents C03DB01 amiloride C05 Vasoprotectives C05A Antihemorrhoidals for topical use C05A antihemorrhoidal preparation: local anaesthetic, astringent, and anti-inﬂammatory medicine* C07 Beta blocking agents C07A Beta blocking agents C07AA Beta blocking agents, non-selective C07AA05 propranolol C07AB Beta blocking agents, selective C07AB03 atenolol C08 Calcium channel blockers C08C Selective calcium channel blockers with mainly vascular effects C08CA Dihydropyridine derivatives C08CA01 amlodipine C08CA05 nifedipine C08D Selective calcium channel blockers with direct cardiac effects C08DA Phenylalkylamine derivatives C08DA01 verapamil C09 Agents acting on the renin-angiotensin system C09A ACE inhibitors, plain C09AA ACE inhibitors, plain C09AA02 enalapril

97 ATC code ATC group/medicine or item

D DERMATOLOGICALS D01 Antifungals for dermatological use D01A Antifungals for topical use D01AA Antibiotics D01AA01 nystatin D01AC Imidazole and triazole derivatives D01AC02 miconazole D01AE Other antifungals for topical use D01AE02 methylrosanilinium chloride (gentian violet)* D01AE12 salicylic acid D01AE13 selenium sulﬁde D01AE20 benzoic acid + salicylic acid* D01B Antifungals for systemic use D01BA Antifungals for systemic use D01BA01 griseofulvin D02 Emollients and protectives D02A Emollients and protectives D02AB Zinc products D02AB calamine lotion* D02AE Carbamide products D02AE01 urea* D05 Antipsoriatics D05A Antipsoriatics for topical use D05AA coal tar* D05AC Antracen derivatives D05AC01 dithranol D06 Antibiotics and chemotherapeutics for dermatological use D06A Antibiotics for topical use D06AX Other antibiotics for topical use D06AX04 neomycin + bacitracin* D06B Chemotherapeutics for topical use D06BA Sulfonamides D06BA01 silver sulfadiazine D06BB Antivirals D06BB04 podophyllum resin* D07 Corticosteroids, dermatological preparations D07A Corticosteroids, plain D07AA Corticosteroids, weak (group I) D07AA02 hydrocortisone D07AC Corticosteroids, potent (group III) D07AC01 betamethasone

98 ATC code ATC group/medicine or item

D08 Antiseptics and disinfectants D08A Antiseptics and disinfectants D08AC Biguanides and amidines D08AC02 chlorhexidine D08AE Phenol and derivatives D08AE05 chloroxylenol D08AG Iodine products D08AG02 polyvidone iodine D08AX Other antiseptics and disinfectants D08AX chlorine base compound* D08AX06 potassium permanganate D08AX08 ethanol D10 Anti-acne preparations D10A Anti-acne preparations for topical use D10AE Peroxides D10AE01 benzoyl peroxide D10AX Other anti-acne preparations for topical use D10AX05 aluminium diacetate

G GENITO URINARY SYSTEM AND SEX HORMONES G01 Gynecological antiinfectives and antiseptics G01A Antiinfectives and antiseptics, excl. combinations with corticosteroids G01AA Antibiotics G01AA01 nystatin G01AF Imidazole derivatives G01AF02 clotrimazole G02B Contraceptives for topical use G02BA Intrauterine contraceptives G02BA02 copper-containing intrauterine device* G02BB Intravaginal contraceptives G02BB diaphragms* G03 Sex hormones and modulators of the genital system G03A Hormonal contraceptives for systemic use G03AA Progestogens and estrogens, ﬁxed combinations G03AA05 ethinylestradiol + norethisterone* G03AB Progestogens and estrogens, sequential preparations G03AB03 ethinylestradiol + levonorgestrel* G03AC Progestogens G03AC01 norethisterone enantate* G03AC03 levonorgestrel G03AC06 medroxyprogesterone acetate*

99 ATC code ATC group/medicine or item

G03B Androgens G03BA 3-Oxoandrosten (4) derivatives G03BA03 testosterone

G03C Estrogens G03CA Natural and semisynthetic estrogens, plain G03CA01 ethinylestradiol

G03D Progestogens G03DC Estren derivatives G03DC02 norethisterone

G03G Gonadotropins and other ovulation stimulants G03GB Ovulation stimulants, synthetic G03GB02 clomifene

G03X Other sex hormones and modulators of the genital system G03XB Antiprogesterons G03XB01 mifepristone

H SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS H01 Pituitary, hypothalamic hormones and analogues H01B Posterior pituitary lobe hormones H01BB Oxytocin and analogues H01BB02 oxytocin

H02 Corticosteroids for systemic use H02A Corticosteroids for systemic use, plain H02AB Glucocorticoids H02AB02 dexamethasone H02AB06 prednisolone H02AB09 hydrocortisone

H03 Thyroid therapy H03A Thyroid preparations H03AA Thyroid hormones H03AA01 levothyroxine*

H03B Antithyroid preparations H03BA Thiouracils H03BA02 propylthiouracil

H03C Iodine therapy H03CA potassium iodide*

J ANTIINFECTIVES FOR SYSTEMIC USE J01 Antibacterials for systemic use J01A Tetracyclines J01AA Tetracyclines J01AA02 doxycycline

100 ATC code ATC group/medicine or item

J01B Amphenicols J01BA Amphenicols J01BA01 chloramphenicol

J01C Beta-lactam antibacterials, penicillins J01CA Penicillins with extended spectrum J01CA01 ampicillin J01CA04 amoxicillin

J01CE Beta-lactamase sensitive penicillins J01CE01 benzylpenicillin J01CE02 phenoxymethylpenicillin J01CE08 benzathine benzylpenicillin J01CE09 procaine benzylpenicillin*

J01CF Beta-lactamase resistant penicillins J01CF02 cloxacillin

J01CR Combinations of penicillins, incl. beta-lactamase inhibitors J01CR02 amoxicillin + clavulanic acid*

J01D Other beta-lactam antibacterials

J01DD Third-generation cephalosporins J01DD02 ceftazidime J01DD04 ceftriaxone J01DD08 ceﬁxime

J01DH Carbapenems J01DH51 imipenem + cilastatin*

J01E Sulfonamides and trimethoprim J01EA Trimethoprim and derivatives J01EA01 trimethoprim J01EC Intermediate-acting sulfonamides J01EC02 sulfadiazine J01EE Combinations of sulfonamides and trimethoprim, incl. derivatives J01EE01 sulfamethoxazole + trimethoprim J01F Macrolides, lincosamides and streptogramins J01FA Macrolides J01FA01 erythromycin J01FA10 azithromycin J01FF Lincosamides J01FF01 clindamycin J01G Aminoglycoside antibacterials J01GA Streptomycins J01GA01 streptomycin

101 ATC code ATC group/medicine or item

J01GB Other aminoglycosides J01GB03 gentamicin J01GB04 kanamycin J01GB06 amikacin J01M Quinolone antibacterials J01MA Fluoroquinolones J01MA01 ofloxacin J01MA02 ciprofloxacin J01MA12 levofloxacin J01X Other antibacterials J01XA Glycopeptide antibacterials J01XA01 vancomycin J01XD Imidazole derivatives J01XD01 metronidazole J01XE Nitrofuran derivatives J01XE01 nitrofurantoin J01XX Other antibacterials J01XX04 spectinomycin J02 Antimycotics for systemic use J02A Antimycotics for systemic use J02AA Antibiotics J02AA01 amphotericin B J02AC Triazole derivatives J02AC01 fluconazole J02AX Other antimycotics for systemic use J02AX01 flucytosine J04 Antimycobacterials J04A Drugs for treatment of tuberculosis J04AA Aminosalicylic acid and derivatives J04AA01 p-aminosalicylic acid* J04AB Antibiotics J04AB01 cycloserine J04AB02 rifampicin J04AB30 capreomycin J04AC Hydrazides J04AC01 isoniazid J04AD Thiocarbamide derivatives J04AD03 ethionamide J04AK Other drugs for treatment of tuberculosis J04AK01 pyrazinamide J04AK02 ethambutol

102 ATC code ATC group/medicine or item

J04AM Combinations of drugs for treatment of tuberculosis J04AM02 rifampicin + isoniazid* J04AM02 rifampicin + isoniazid + pyrazinamide* J04AM02 rifampicin + isoniazid + pyrazinamide + ethambutol* J04AM03 isoniazid + ethambutol* J04B Drugs for treatment of lepra J04BA Drugs for treatment of lepra J04BA01 clofazimine J04BA02 dapsone J05 Antivirals for systemic use J05A Direct acting antivirals J05AB Nucleosides and nucleotides excl. reverse transcriptase inhibitors J05AB01 aciclovir J05AE Protease inhibitors J05AE01 saquinavir (SQV) J05AE02 indinavir (IDV) J05AE03 ritonavir (r) J05AE04 nelﬁnavir (NFV) J05AE30 lopinavir + ritonavir (LPV/r)*

J05AF Nucleoside reverse transcriptase inhibitors J05AF01 zidovudine (ZDV or AZT) J05AF02 didanosine (ddI) J05AF04 stavudine (d4T) J05AF05 lamivudine (3TC) J05AF06 abacavir (ABC)

J05AG Non-nucleoside reverse transcriptase inhibitors J05AG01 nevirapine (NVP) J05AG03 efavirenz (EFV or EFZ)

J06 Immune sera and immunoglobulins J06A Immune sera J06AA Immune sera J06AA01 diphtheria antitoxin J06AA03 antivenom sera*

J06B Immunoglobulins J06BB Speciﬁc immunoglobulins J06BB01 anti-D immunoglobulin (human) J06BB02 antitetanus immunoglobulin (human) J06BB05 rabies immunoglobulin

J07 Vaccines J07A Bacterial vaccines J07AH meningococcal meningitis vaccine*

103 ATC code ATC group/medicine or item

J07AJ Pertussis vaccines J07AJ51 diphtheria-pertussis-tetanus vaccine* J07AM Tetanus vaccines J07AM51 diphtheria-tetanus vaccine* J07AN Tuberculosis vaccines J07AN01 BCG vaccine* J07AP typhoid vaccine J07B Viral vaccines J07BB inﬂuenza vaccine J07BC Hepatitis vaccines J07BC01 hepatitis B vaccine J07BD measles vaccine* J07BD52 measles-mumps-rubella vaccine* J07BF poliomyelitis vaccine J07BG rabies vaccine J07BJ rubella vaccine J07BL yellow fever vaccine

L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS L01 Antineoplastic agents L01A Alkylating agents L01AA Nitrogen mustard analogues L01AA01 cyclophosphamide L01AA02 chlorambucil L01AA05 chlormethine L01AX Other alkylating agents L01AX04 dacarbazine L01B Antimetabolites L01BA Folic acid analogues L01BA01 methotrexate L01BB Purine analogues L01BB02 mercaptopurine L01BC Pyrimidine analogues L01BC01 cytarabine L01BC02 ﬂuorouracil L01C Plant alkaloids and other natural products L01CA Vinca alkaloids and analogues L01CA01 vinblastine L01CA02 vincristine L01CB Podophyllotoxin derivatives L01CB01 etoposide

104 ATC code ATC group/medicine or item

L01D Cytotoxic antibiotics and related substances L01DA Actinomycines L01DA01 dactinomycin L01DB Anthracyclines and related substances L01DB01 doxorubicin L01DB02 daunorubicin L01DC Other cytotoxic antibiotics L01DC01 bleomycin L01X Other antineoplastic agents L01XA Platinum compounds L01XA01 cisplatin L01XB Methylhydrazines L01XB01 procarbazine L01XX Other antineoplastic agents L01XX02 asparaginase L02 Endocrine therapy L02B Hormone antagonists and related agents L02BA Anti-estrogens L02BA01 tamoxifen L04 Immunosuppressive agents L04A Immunosuppressive agents L04AA Selective immunosuppressive agents L04AA01 ciclosporin L04AX Other immunosuppressive agents L04AX01 azathioprine

M MUSCULO-SKELETAL SYSTEM M01 Antiinflammatory and antirheumatic products M01A Antiinflammatory and antirheumatic products, non-steroids M01AE Propionic acid derivatives M01AE01 ibuprofen M01C Specific antirheumatic agents M01CC Penicillamine and similar agents M01CC01 penicillamine M03 Muscle relaxants M03A Muscle relaxants, peripherally acting agents M03AA Curare alkaloids M03AA01 alcuronium M03AB Choline derivatives M03AB01 suxamethonium M03AC Other quaternary ammonium compounds M03AC03 vecuronium

105 ATC code ATC group/medicine or item

M04 Antigout preparations M04A Antigout preparations M04AA Preparations inhibiting uric acid production M04AA01 allopurinol

N NERVOUS SYSTEM N01 Anesthetics N01A Anesthetics, general N01AB Halogenated hydrocarbons N01AB01 halothane N01AF Barbiturates, plain N01AF03 thiopental N01AX Other general anesthetics N01AX03 ketamine N01AX13 nitrous oxide N01B Anesthetics, local N01BB Amides N01BB01 bupivacaine N01BB02 lidocaine N01BB52 lidocaine + epinephrine (adrenaline)* N02 Analgesics N02A Opioids N02AA Natural opium alkaloids N02AA01 morphine N02B Other analgesics and antipyretics N02BA Salicylic acid and derivatives N02BA01 acetylsalicylic acid N02BE Anilides N02BE01 paracetamol N03 Antiepileptics N03A Antiepileptics N03AA Barbiturates and derivatives N03AA02 phenobarbital N03AB Hydantoin derivatives N03AB02 phenytoin N03AD Succinimide derivatives N03AD01 ethosuximide N03AF Carboxamide derivatives N03AF01 carbamazepine N03AG Fatty acid derivatives N03AG01 valproic acid

106 ATC code ATC group/medicine or item

N04 Anti-parkinson drugs N04A Anticholinergic agents N04AA Tertiary amines N04AA02 biperiden N04B Dopaminergic agents N04BA Dopa and dopa derivatives N04BA02 levodopa + carbidopa* N05 Psycholeptics N05A Antipsychotics N05AA Phenothiazines with aliphatic side-chain N05AA01 chlorpromazine N05AB Phenothiazines with piperazine structure N05AB02 ﬂuphenazine N05AD Butyrophenone derivatives N05AD01 haloperidol N05AN Lithium N05AN01 lithium carbonate* N05B Anxiolytics N05BA Benzodiazepine derivatives N05BA01 diazepam N06 Psychoanaleptics N06A Antidepressants N06AA Non-selective monoamine reuptake inhibitors N06AA04 clomipramine N06AA09 amitriptyline N07 Other nervous system drugs N07A Parasympathomimetics N07AA Anticholinesterases N07AA01 neostigmine N07AA02 pyridostigmine N07B Drugs used in addictive disorders N07BC Drugs used in opioid dependence N07BC01 buprenorphine N07BC02 methadone

P ANTIPARASITIC PRODUCTS, INSECTICIDES AND REPELLENTS P01 Antiprotozoals P01A Agents against amoebiasis and other protozoal diseases P01AB Nitroimidazole derivatives P01AB01 metronidazole

107 ATC code ATC group/medicine or item

P01AC Dichloroacetamide derivatives P01AC01 diloxanide P01B Antimalarials P01BA Aminoquinolines P01BA01 chloroquine P01BA03 primaquine P01BA06 amodiaquine P01BB Biguanides P01BB01 proguanil P01BC Methanolquinolines P01BC01 quinine P01BC02 meﬂoquine P01BD Diaminopyrimidines P01BD01 pyrimethamine P01BD51 sulfadoxine + pyrimethamine* P01BE Artemisinin and derivatives P01BE02 artemether P01BE03 artesunate P01BE52 artemether + lumefantrine* P01C Agents against leishmaniasis and trypanosomiasis P01CA Nitroimidazole derivatives P01CA02 benznidazole P01CB Antimony compounds P01CB01 meglumine antimoniate P01CC Nitrofuran derivatives P01CC01 nifurtimox P01CD Arsenic compounds P01CD01 melarsoprol P01CX Other agents against leishmaniasis and trypanosomiasis P01CX01 pentamidine* P01CX02 suramin sodium P01CX03 eﬂornithine P02 Anthelmintics P02B Antitrematodals P02BA Quinoline derivatives and related substances P02BA01 praziquantel P02BA02 oxamniquine P02BX Other antitrematodal agents P02BX04a triclabendazole

a Provisional code pending formal approval by the WHO International Working Group for Drug Statistics Methodology, Oslo, Norway.

108 ATC code ATC group/medicine or item

P02C Antinematodal agents P02CA Benzimidazole derivatives P02CA01 mebendazole P02CA03 albendazole P02CB Piperazine and derivatives P02CB02 diethylcarbamazine P02CC Tetrahydropyrimidine derivatives P02CC01 pyrantel P02CE Imidazothiazole derivatives P02CE01 levamisole P02CF Avermectines P02CF01 ivermectin P02D Anticestodals P02DA Salicylic acid derivatives P02DA01 niclosamide P03 Ectoparasiticides, incl. scabicides, insecticides and repellents P03A Ectoparasiticides, incl. scabicides P03AC Pyrethrines, incl. synthetic compounds P03AC04 permethrin P03AX Other ectoparasiticides, incl. scabicides P03AX01 benzyl benzoate

R RESPIRATORY SYSTEM R03 Drugs for obstructive airway diseases R03A Adrenergics, inhalants R03AC Selective beta-2-adrenoreceptor agonists R03AC02 salbutamol R03B Other drugs for obstructive airway diseases, inhalants R03BA Glucocorticoids R03BA01 beclometasone R03BB Anticholinergics R03BB01 ipratropium bromide R03C Adrenergics for systemic use R03CA Alpha- and beta-adrenoreceptor agonists R03CA02 ephedrine R03CC Selective beta-2-adrenoreceptor agonists R03CC02 salbutamol R05 Cough and cold preparations R05D Cough suppressants, excl. combinations with expectorants R05DA Opium alkaloids and derivatives R05DA04 codeine

109 ATC code ATC group/medicine or item

R06 Antihistamines for systemic use R06A Antihistamines for systemic use R06AB Substituted alkylamines R06AB04 chlorphenamine R06AD Phenothiazine derivatives R06AD02 promethazine

S SENSORY ORGANS S01 Ophthalmologicals S01A Antiinfectives S01AA Antibiotics S01AA09 tetracycline S01AA11 gentamicin S01AD Antivirals S01AD01 idoxuridine S01B Antiinﬂammatory agents S01BA Corticosteroids, plain S01BA04 prednisolone S01E Antiglaucoma preparations and miotics S01EA Sympathomimetics in glaucoma therapy S01EA01 epinephrine S01EB Parasympathomimetics S01EB01 pilocarpine S01EC Carbonic anhydrase inhibitors S01EC01 acetazolamide S01ED Beta blocking agents S01ED01 timolol S01F Mydriatics and cycloplegics S01FA Anticholinergics S01FA01 atropine S01FA06 tropicamide S01H Local anesthetics S01HA Local anesthetics S01HA03 tetracaine S01J Diagnostic agents S01JA Colouring agents S01JA01 ﬂuorescein

V VARIOUS V03 All other therapeutic products V03A All other therapeutic products V03AB Antidotes V03AB03 sodium calcium edetate*

110 ATC code ATC group/medicine or item

V03AB06 sodium thiosulfate* V03AB08 sodium nitrite V03AB09 dimercaprol V03AB14 protamine sulfate* V03AB15 naloxone V03AB17 methylthioninium chloride (methylene blue) V03AB23 acetylcysteine V03AB26 DL-methionine*

V03AB31 potassium ferric hexacyanoferrate (II).2H2O (Prussian blue) V03AC Iron chelating agents V03AC01 deferoxamine V03AF Detoxifying agents for antineoplastic treatment V03AF03 calcium folinate V03AN Medical gases V03AN oxygen V04 Diagnostic agents V04C Other diagnostic agents V04CF Tuberculosis diagnostics V04CF01 tuberculin, puriﬁed protein derivative (PPD)* V07 All other non-therapeutic products V07A All other non-therapeutic products V07AB Solvents and diluting agents, incl. irrigating solutions V07AB water for injection* V07AV Technical disinfectants V07AV glutaral V08 Contrast media V08A X-ray contrast media, iodinated V08AA Watersoluble, nephrotropic, high osmolar X-ray contrast media V08AA01 amidotrizoate* V08AB Watersoluble, nephrotropic, low osmolar X-ray contrast media V08AB02 iohexol V08AC Watersoluble, hepatotropic X-ray contrast media V08AC02 meglumine iotroxate* V08AC06 iopanoic acid V08AD Non-watersoluble X-ray contrast media V08AD03 propyliodone V08B X-ray contrast media, non-iodinated V08BA Barium sulfate containing X-ray contrast media V08BA01 barium sulfate*

* Medicine or item name differs slightly from the name used in the ATC classiﬁcation system.

111 Alphabetical list of essential medicines (with ATC classiﬁcation code numbers)

Medicine or item ATC code Section abacavir (ABC) J05AF06 6.4.2a acetazolamide S01EC01 21.4 acetylcysteine V03AB23 4.2 acetylsalicylic acid B01AC06 12.5 acetylsalicylic acid N02BA01 22.1; 7.1 aciclovir J05AB01 6.4.1 albendazole P02CA03 6.1.1 alcuronium M03AA01 20 allopurinol M04AA01 2.3 aluminium diacetate D11AA 13.4 aluminium hydroxide A02AB01 17.1 amidotrizoate* V08AA01 14.2 amikacin J01GB06 6.2.4 amiloride C03DB01 16 p-aminosalicylic acid* J04AA01 6.2.4 amitriptyline N06AA09 24.2.1 amlodipine C08CA01 amodiaquine P01BA06 6.5.3a amoxicillin J01CA04 6.2.1 amoxicillin + clavulanic acid* J01CR02 6.2.1 amphotericin B J02AA01 6.3; 6.5.2 ampicillin J01CA01 6.2.1 anti-D immunoglobulin (human) J06BB01 19.2 antihaemorrhoidal preparation: C05A 17.3 local anaesthetic, astringent, and anti-inﬂammatory drug* antitetanus immunoglobulin (human)* J06BB02 19.2 antivenom sera* J06AA03 19.2 artemether P01BE02 6.5.3a artemether + lumefantrine* P01BE52 6.5.3a artesunate P01BE03 6.5.3a ascorbic acid A11GA01 27 asparaginase L01XX02 8.2 atenolol C07AB03 12.1; 12.2; 12.3 atropine A03BA01 1.3; 4.2 atropine S01FA01 21.5 azathioprine L04AX01 2.4; 8.1 azithromycin J01FA10 6.2.2

barium sulfate* V08BA01 14.2 BCG vaccine* J07AN01 19.3.1 beclometasone R03BA01 25.1 benzathine benzylpenicillin J01CE08 6.2.1 benznidazole P01CA02 6.5.5b benzoic acid + salicylic acid* D01AE20 13.1

112 Medicine or item ATC code Section benzoyl peroxide D10AE01 13.5 benzyl benzoate P03AX01 13.6 benzylpenicillin J01CE01 6.2.1 betamethasone D07AC01 13.3 biperiden N04AA02 9 bleomycin L01DC01 8.2 bupivacaine N01BB01 1.2 buprenorphine N07BC01 calamine lotion* D02AB 13.3 calcium folinate V03AF03 8.2 calcium gluconate A12AA03 4.2; 27 capreomycin J04AB30 6.2.4 carbamazepine N03AF01 5; 24.2.2 ceﬁxime J01DD08 ceftazidime J01DA11 6.2.1 ceftriaxone J01DA13 6.2.1 charcoal, activated* A07BA01 4.1 chlorambucil L01AA02 8.2 chloramphenicol J01BA01 6.2.2 chlorhexidine D08AC02 15.1 chlorine base compound* D08AX 15.2 chlormethine L01AA05 8.2 chloroquine P01BA01 2.4; 6.5.3a; 6.5.3.b chloroxylenol D08AE05 15.2 chlorphenamine R06AB04 3 chlorpromazine N05AA01 24.1 ciclosporin L04AA01 8.1 ciproﬂoxacin J01MA02 6.2.2; 6.2.4 cisplatin L01XA01 8.2 clindamycin J01FF01 6.2.2 clofazimine J04BA01 6.2.3 clomifene G03GB02 18.6 clomipramine N06AA04 24.4 clotrimazole G01AF02 coal tar* D05AA 13.5 codeine R05DA04 2.2; 17.7.2 condoms 18.3.3 copper-containing intrauterine device* G02BA02 18.3.2 cyclophosphamide L01AA01 8.2 cycloserine J04AB01 6.2.4 cytarabine L01BC01 8.2 dacarbazine L01AX04 8.2 dactinomycin L01DA01 8.2 dapsone J04BA02 6.2.3 daunorubicin L01DB02 8.2 deferoxamine V03AC01 4.2

113 Medicine or item ATC code Section dexamethasone H02AB02 3; 8.3 dextran 70* B05AA05 11.1 diaphragms G02BB 18.3.3 diazepam N05BA01 1.3; 5; 24.3 dicloxacillin J01CF01 6.2.1 didanosine (ddI) J05AF02 6.4.2a diethylcarbamazine P02CB02 6.1.2 digoxin C01AA05 12.2; 12.4 diloxanide P01AC01 6.5.1 dimercaprol V03AB09 4.2 diphtheria-pertussis-tetanus vaccine* J07AJ51 19.3.1 diphtheria antitoxin J06AA01 19.2 diphtheria-tetanus vaccine* J07AM51 19.3.1 dithranol D05AC01 13.5 dopamine C01CA04 12.4 doxorubicin L01DB01 8.2 doxycycline J01AA02 6.2.2; 6.5.3b; 6.5.3a

efavirenz (EFV or EFZ) J05AG03 6.4.2b eﬂornithine P01CX03 6.5.5a enalapril C09AA02 12.3 ephedrine R03CA02 1.2 epinephrine (adrenaline) C01CA24 3; 25.1; 12.2 epinephrine (adrenaline) S01EA01 21.5 ergocalciferol A11CC01 27 erythromycin J01FA01 6.2.2 ethambutol J04AK02 6.2.4 ethanol D08AX08 15.1 ethinylestradiol G03CA01 18.4 ethinylestradiol + levonorgestrel* G03AB03 18.3.1 ethinylestradiol + norethisterone* G03AA05 18.3.1 ethionamide J04AD03 6.2.4 ethosuximide N03AD01 5 etoposide L01CB01 8.2

factor IX complex (coagulation factors II, VII, B02BD01 11.2 IX,X) concentrate* factor VIII concentrate* B02BD02 11.2 ferrous salt* B03A 10.1 ferrous salt + folic acid* B03AD 10.1 fluconazole J02AC01 6.3 flucytosine J02AX01 6.3 fluorescein S01JA01 14.1 fluorouracil L01BC02 13.5; 8.2 fluphenazine N05AB02 24.1 folic acid B03BB01 10.1 furosemide C03CA01 16

114 Medicine or item ATC code Section gentamicin J01GB03 6.2.2 gentamicin S01AA11 21.1 glibenclamide A10BB01 18.5 glucose* B05BA03 26.2 glucose with sodium chloride* B05BB02 26.2 glutaral V07AV 15.2 glyceryl trinitrate C01DA02 12.1 griseofulvin D01BA01 6.3 haloperidol N05AD01 24.1 halothane N01AB01 1.1 heparin sodium* B01AB01 10.2 hepatitis B vaccine J07BC01 19.3.1 hydralazine C02DB02 12.3 hydrochlorothiazide C03AA03 12.3; 12.4; 16 hydrocortisone A07EA02 17.4 hydrocortisone D07AA02 13.3 hydrocortisone H02AB09 3; 8.3 hydroxocobalamin B03BA03 10.1 ibuprofen M01AE01 2.1 idoxuridine S01AD01 21.1 imipenem + cilastatin* J01DH51 6.2.1 indinavir (IDV) J05AE02 6.4.2c inﬂuenza vaccine J07BB 19.3.2 insulin injection (soluble)* A10AB 18.5 insulin, intermediate-acting* A10AC 18.5 intraperitoneal dialysis solution* B05DA 23 iodine* A12CX 27 iohexol V08AB02 14.2 iopanoic acid V08AC06 14.2 ipratropium bromide R03BB01 25.1 isoniazid J04AC01 6.2.4 isoniazid + ethambutol* J04AM03 6.2.4 isosorbide dinitrate C01DA08 12.1 ivermectin P02CF01 6.1.2 kanamycin J01GB04 6.2.4 ketamine N01AX03 1.1 lamivudine (3TC) J05AF05 6.4.2a levamisole P02CE01 6.1.1; 8.2 levodopa + carbidopa* N04BA02 9 levoﬂoxacin J01MA12 6.2.4 levonorgestrel G03AC03 18.3.1 levothyroxine* H03AA01 18.8 lidocaine C01BB01 12.2 lidocaine N01BB02 1.2 lidocaine + epinephrine (adrenaline)* N01BB52 1.2

115 Medicine or item ATC code Section lithium carbonate* N05AN01 24.2.2 lopinavir + ritonavir (LPV/r)* J05AE30 6.4.2c magnesium hydroxide A02AA04 17.1 magnesium sulfate B05XA05 5 mannitol B05BC01 16 measles-mumps-rubella vaccine* J07BD52 19.3 mebendazole P02CA01 6.1.1 medroxyprogesterone acetate* G03AC06 18.3.1; 18.7 meﬂoquine P01BC02 6.5.3a meglumine antimoniate P01CB01 6.5.2 meglumine iotroxate* V08AC02 14.2 melarsoprol P01CD01 6.5.5 meningococcal meningitis vaccine* J07AH 19.3.2 mercaptopurine L01BB02 8.2 metformin A10BA02 18.5 methadone N07BC02 DL-methionine* V03AB26 4.2 methotrexate L01BA01 2.4; 8.2 methyldopa* C02AB01 12.3 methylrosanilinium chloride (gentian violet)* D01AE02 13.2 methylthioninium chloride (methylene blue) V03AB17 4.2 metoclopramide A03FA01 17.2 metronidazole J01XD01 6.2.2 metronidazole P01AB01 6.5.1 miconazole D01AC02 13.1 mifepristone G03XB01 misoprostol A02BB01 morphine N02AA01 1.3; 2.2

naloxone V03AB15 4.2 nelﬁnavir (NFV) J05AE04 6.4.2c neomycin + bacitracin* D06AX30 13.2 neostigmine N07AA01 20 nevirapine (NVP) J05AG01 6.4.2b niclosamide P02DA01 6.1.1 nicotinamide A11HA01 27 nifedipine C08CA05 12.3 nifurtimox P01CC01 6.5.5b nitrofurantoin J01XE01 6.2.2 nitrous oxide N01AX13 1.1 norethisterone G03DC02 18.7 norethisterone enantate* G03AC01 18.3.1 nystatin A07AA02 6.3 nystatin D01AA01 6.3 nystatin G01AA01 6.3 oﬂoxacin J01MA01 6.2.4 oral rehydration salts (for glucose–electrolyte A07CA 17.7.1; 26.1 solution)*

116 Medicine or item ATC code Section oxamniquine P02BA02 6.1.3 oxygen V03AN 1.1 oxytocin H01BB02 22.1 paracetamol N02BE01 2.1; 7.1 penicillamine M01CC01 2.2; 4.2 pentamidne* P01CX01 6.5.1; 6.5.4; 6.5.5a permethrin P03AC04 13.6 phenobarbital N03AA02 5 phenoxymethylpenicillin J01CE02 6.2.1 phenytoin N03AB02 5 phytomenadione B02BA01 10.2 pilocarpine S01EB01 21.4 podophyllum resin* D06BB04 13.5 poliomyelitis vaccine J07BF 19.3.1 polyvidone iodine* D08AG02 15.1 potassium chloride B05XA01 26.1; 26.2 potassium ferric hexacyanoferrate (II).2H2O V03AB31 4.2 (Prussian blue) potassium iodide* H03CA 18.8; 6.3 potassium permanganate D08AX06 13.2 praziquantel P02BA01 6.1.1; 6.1.3 prednisolone H02AB06 3; 8.3 prednisolone S01BA04 21.2 primaquine P01BA03 6.5.3a procainamide C01BA02 12.2 procaine benzylpenicillin* J01CE09 6.2.1 procarbazine L01XB01 8.2 proguanil P01BB01 6.5.3b promethazine R06AD02 1.3; 17.2 propranolol C07AA05 7.2 propyliodone V08AD03 14.2 propylthiouracil H03BA02 18.8 protamine sulfate* V03AB14 10.2 pyrantel P02CC01 6.1.1 pyrazinamide J04AK01 6.2.4 pyridostigmine N07AA02 20 pyridoxine A11HA02 27 pyrimethamine P01BD01 6.5.4 quinidine C01BA01 12.2 quinine P01BC01 6.5.3a rabies immunoglobulin J06BB05 19.2 rabies vaccine J07BG 19.3.2 ranitidine A02BA02 17.1 retinol A11CA01 27 riboﬂavin A11HA04 27

117 Medicine or item ATC code Section rifampicin J04AB02 6.2.3; 6.2.4 rifampicin + isoniazid* J04AM02 6.2.4 rifampicin + isoniazid + pyrazinamide* J04AM02 6.2.4 rifampicin + isoniazid + pyrazinamide + J04AM02 6.2.4 ethambutol* ritonavir (r) J05AE03 6.4.2c rubella vaccine J07BJ 19.3.2

salbutamol R03AC02 25.1 salbutamol R03CC02 25.1 salicylic acid D01AE12 13.5 saquinavir (SQV) J05AE01 6.4.2c selenium sulﬁde D01AE13 13.1 senna* A06AB06 17.6 silver sulfadiazine D06BA01 13.2 sodium calcium edetate* V03AB03 4.2 sodium chloride B05XA03 26.2 sodium ﬂuoride A12CD01 27 sodium hydrogen carbonate* B05XA02 26.2 sodium lactate, compound solution* B05BB01 26.2 sodium nitrite V03AB08 4.2 sodium nitroprusside* C02DD01 12.3 sodium thiosulfate* V03AB06 4.2; 13.1 spectinomycin J01XX04 6.2.2 spironolactone C03DA01 16 stavudine (d4T) J05AF04 6.4.3a streptokinase B01AD01 12.5 streptomycin J01GA01 6.2.4 sulfadiazine J01EC02 6.2.2 sulfadoxine + pyrimethamine* P01BD51 6.5.3a sulfamethoxazole + trimethoprim J01EE01 6.2.2; 6.5.4 sulfasalazine A07EC01 2.4; 17.4 suramin sodium P01CX02 6.5.5a; 6.1.2 suxamethonium M03AB01 20

tamoxifen L02BA01 8.3 testosterone G03BA03 18.2 tetracaine S01HA03 21.3 tetracycline S01AA09 21.1 thiamine A11DA01 27 thiopental N01AF03 1.1 timolol S01ED01 21.4 triclabendazole P02BX04a 6.1.3 trimethoprim J01EA01 6.2.2 tropicamide S01FA06 14.1 tuberculin, puriﬁed protein derivative (PPD)* V04CF01 19.1 typhoid vaccine J07AP 19.3.2

urea* D02AE01 13.5

118 Medicine or item ATC code Section valproic acid N03AG01 5; 24.2.2 vancomycin J01XA01 6.2.2 vecuronium M03AC03 20 verapamil C08DA01 12.1; 12.2 vinblastine L01CA01 8.2 vincristine L01CA02 8.2

warfarin B01AA03 10.2 water for injection* V07AB 26.3

yellow fever vaccine J07BL 19.3.2

zidovudine (ZDV or AZT) J05AF01 6.4.2a zinc sulfate A12CB01

* Medicine or item name differs slightly from the name used in the ATC classiﬁcation system. a Provisional code pending formal approval by the WHO International Working Group for Drug Statistics Methodology.

119